Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
7 | g.55181287_55181299delinsCTCCAGGAAGCCT | CA1708904901 | EGFR,EGFR-AS1 | c.2125-6_2131delinsCTCCAGGAAGCCT c.633-6_639delinsCTCCAGGAAGCCT c.2284-6_2290delinsCTCCAGGAAGCCT c.*28+8359_*28+8371delinsCTCCAGGAAGCCT (n.*28+8359_*28+8371delinsCTCCAGGAAGCCT) c.2149-6_2155delinsCTCCAGGAAGCCT n.1272_1284delinsAGGCTTCCTGGAG c.1483-6_1489delinsCTCCAGGAAGCCT | |
7 | g.55181288_55181299del | CA135832 | EGFR,EGFR-AS1 | c.2125-5_2131del c.633-5_639del c.2284-5_2290del c.*28+8360_*28+8371del (n.*28+8360_*28+8371del) c.2149-5_2155del n.1272_1283del c.1483-5_1489del | ClinVar dbSNP |
7 | g.55181288_55181299dup | CA135833 | EGFR,EGFR-AS1 | c.2125-5_2131dup c.633-5_639dup c.2284-5_2290dup c.*28+8360_*28+8371dup (n.*28+8360_*28+8371dup) c.2149-5_2155dup n.1272_1283dup c.1483-5_1489dup | ClinVar dbSNP COSMIC |
7 | g.55181294A>C | CA367578490 | EGFR,EGFR-AS1 | c.2126A>C (p.Glu709Ala) c.634A>C c.2285A>C (p.Glu762Ala) c.*28+8366A>C (n.*28+8366A>C) c.2150A>C (p.Glu717Ala) n.1277T>G c.1484A>C (p.Glu495Ala) | |
7 | g.55181294A>G | CA367578492 | EGFR,EGFR-AS1 | c.2126A>G (p.Glu709Gly) c.634A>G c.2285A>G (p.Glu762Gly) c.*28+8366A>G (n.*28+8366A>G) c.2150A>G (p.Glu717Gly) n.1277T>C c.1484A>G (p.Glu495Gly) | |
7 | g.55181294A>T | CA367578494 | EGFR,EGFR-AS1 | c.2126A>T (p.Glu709Val) c.634A>T c.2285A>T (p.Glu762Val) c.*28+8366A>T (n.*28+8366A>T) c.2150A>T (p.Glu717Val) n.1277T>A c.1484A>T (p.Glu495Val) | dbSNP |
7 | g.55181295A>C | CA367578496 | EGFR,EGFR-AS1 | c.2127A>C (p.Glu709Asp) c.635A>C c.2286A>C (p.Glu762Asp) c.*28+8367A>C (n.*28+8367A>C) c.2151A>C (p.Glu717Asp) n.1276T>G c.1485A>C (p.Glu495Asp) | dbSNP |
7 | g.55181295A>G | CA455165011 | EGFR,EGFR-AS1 | c.2127A>G (p.Glu709=) c.635A>G c.2286A>G (p.Glu762=) c.*28+8367A>G (n.*28+8367A>G) c.2151A>G (p.Glu717=) n.1276T>C c.1485A>G (p.Glu495=) | ClinVar dbSNP |
7 | g.55181295A>T | CA367578498 | EGFR,EGFR-AS1 | c.2127A>T (p.Glu709Asp) c.635A>T c.2286A>T (p.Glu762Asp) c.*28+8367A>T (n.*28+8367A>T) c.2151A>T (p.Glu717Asp) n.1276T>A c.1485A>T (p.Glu495Asp) | dbSNP |
7 | g.55181296G>A | CA367578501 | EGFR,EGFR-AS1 | c.2128G>A (p.Ala710Thr) c.636G>A c.2287G>A (p.Ala763Thr) c.*28+8368G>A (n.*28+8368G>A) c.2152G>A (p.Ala718Thr) n.1275C>T c.1486G>A (p.Ala496Thr) | ClinVar dbSNP |
7 | g.55181296G>C | CA367578503 | EGFR,EGFR-AS1 | c.2128G>C (p.Ala710Pro) c.636G>C c.2287G>C (p.Ala763Pro) c.*28+8368G>C (n.*28+8368G>C) c.2152G>C (p.Ala718Pro) n.1275C>G c.1486G>C (p.Ala496Pro) | dbSNP |
7 | g.55181296G>T | CA367578505 | EGFR,EGFR-AS1 | c.2128G>T (p.Ala710Ser) c.636G>T c.2287G>T (p.Ala763Ser) c.*28+8368G>T (n.*28+8368G>T) c.2152G>T (p.Ala718Ser) n.1275C>A c.1486G>T (p.Ala496Ser) | |
7 | g.55181297C>A | CA367578512 | EGFR,EGFR-AS1 | c.2129C>A (p.Ala710Asp) c.637C>A c.2288C>A (p.Ala763Asp) c.*28+8369C>A (n.*28+8369C>A) c.2153C>A (p.Ala718Asp) n.1274G>T c.1487C>A (p.Ala496Asp) | dbSNP |
7 | g.55181297C= | CA1708904938 | EGFR,EGFR-AS1 | c.2129C= (p.Ala710=) c.637C= c.2288C= (p.Ala763=) c.*28+8369C= (n.*28+8369C=) c.2153C= (p.Ala718=) n.1274G= c.1487C= (p.Ala496=) | |
7 | g.55181297C>G | CA367578508 | EGFR,EGFR-AS1 | c.2129C>G (p.Ala710Gly) c.637C>G c.2288C>G (p.Ala763Gly) c.*28+8369C>G (n.*28+8369C>G) c.2153C>G (p.Ala718Gly) n.1274G>C c.1487C>G (p.Ala496Gly) | dbSNP |
7 | g.55181297C>T | CA367578510 | EGFR,EGFR-AS1 | c.2129C>T (p.Ala710Val) c.637C>T c.2288C>T (p.Ala763Val) c.*28+8369C>T (n.*28+8369C>T) c.2153C>T (p.Ala718Val) n.1274G>A c.1487C>T (p.Ala496Val) | ClinVar dbSNP gnomAD v2 gnomAD v4 COSMIC |
7 | g.55181298del | CA2573142219 | EGFR,EGFR-AS1 | c.2130del (p.Tyr711ThrfsTer2) c.638del c.2289del (p.Tyr764ThrfsTer2) c.*28+8370del (n.*28+8370del) c.2154del (p.Tyr719ThrfsTer2) n.1274del c.1488del (p.Tyr497ThrfsTer2) | ClinVar dbSNP |
7 | g.55181298C>A | CA455165074 | EGFR,EGFR-AS1 | c.2130C>A (p.Ala710=) c.638C>A c.2289C>A (p.Ala763=) c.*28+8370C>A (n.*28+8370C>A) c.2154C>A (p.Ala718=) n.1273G>T c.1488C>A (p.Ala496=) | dbSNP |
7 | g.55181298C= | CA1708904942 | EGFR,EGFR-AS1 | c.2130C= (p.Ala710=) c.638C= c.2289C= (p.Ala763=) c.*28+8370C= (n.*28+8370C=) c.2154C= (p.Ala718=) n.1273G= c.1488C= (p.Ala496=) | |
7 | g.55181298C>G | CA135834 | EGFR,EGFR-AS1 | c.2130C>G (p.Ala710=) c.638C>G c.2289C>G (p.Ala763=) c.*28+8370C>G (n.*28+8370C>G) c.2154C>G (p.Ala718=) n.1273G>C c.1488C>G (p.Ala496=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.55181298C>T | CA455165075 | EGFR,EGFR-AS1 | c.2130C>T (p.Ala710=) c.638C>T c.2289C>T (p.Ala763=) c.*28+8370C>T (n.*28+8370C>T) c.2154C>T (p.Ala718=) n.1273G>A c.1488C>T (p.Ala496=) | ClinVar dbSNP |
7 | g.55181299T>A | CA367578516 | EGFR,EGFR-AS1 | c.2131T>A (p.Tyr711Asn) c.639T>A c.2290T>A (p.Tyr764Asn) c.*28+8371T>A (n.*28+8371T>A) c.2155T>A (p.Tyr719Asn) n.1272A>T c.1489T>A (p.Tyr497Asn) | dbSNP |
7 | g.55181299T>C | CA367578518 | EGFR,EGFR-AS1 | c.2131T>C (p.Tyr711His) c.639T>C c.2290T>C (p.Tyr764His) c.*28+8371T>C (n.*28+8371T>C) c.2155T>C (p.Tyr719His) n.1272A>G c.1489T>C (p.Tyr497His) | dbSNP |
7 | g.55181299T>G | CA367578520 | EGFR,EGFR-AS1 | c.2131T>G (p.Tyr711Asp) c.639T>G c.2290T>G (p.Tyr764Asp) c.*28+8371T>G (n.*28+8371T>G) c.2155T>G (p.Tyr719Asp) n.1272A>C c.1489T>G (p.Tyr497Asp) | |
7 | g.55181299T= | CA1708904949 | EGFR,EGFR-AS1 | c.2131T= (p.Tyr711=) c.639T= c.2290T= (p.Tyr764=) c.*28+8371T= (n.*28+8371T=) c.2155T= (p.Tyr719=) n.1272A= c.1489T= (p.Tyr497=) | |
7 | g.55181300A>C | CA367578524 | EGFR,EGFR-AS1 | c.2132A>C (p.Tyr711Ser) c.640A>C c.2291A>C (p.Tyr764Ser) c.*28+8372A>C (n.*28+8372A>C) c.2156A>C (p.Tyr719Ser) n.1271T>G c.1490A>C (p.Tyr497Ser) | dbSNP |
7 | g.55181300A>G | CA367578527 | EGFR,EGFR-AS1 | c.2132A>G (p.Tyr711Cys) c.640A>G c.2291A>G (p.Tyr764Cys) c.*28+8372A>G (n.*28+8372A>G) c.2156A>G (p.Tyr719Cys) n.1271T>C c.1490A>G (p.Tyr497Cys) | dbSNP |
7 | g.55181300A>T | CA367578529 | EGFR,EGFR-AS1 | c.2132A>T (p.Tyr711Phe) c.640A>T c.2291A>T (p.Tyr764Phe) c.*28+8372A>T (n.*28+8372A>T) c.2156A>T (p.Tyr719Phe) n.1271T>A c.1490A>T (p.Tyr497Phe) | dbSNP |
7 | g.55181301_55181302insCACCAC | CA2573051277 | EGFR,EGFR-AS1 | c.2133_2134insCACCAC (p.Tyr711_Val712insHisHis) c.641_642insCACCAC c.2292_2293insCACCAC (p.Tyr764_Val765insHisHis) c.*28+8373_*28+8374insCACCAC (n.*28+8373_*28+8374insCACCAC) c.2157_2158insCACCAC (p.Tyr719_Val720insHisHis) n.1271_1272insGGTGGT c.1491_1492insCACCAC (p.Tyr497_Val498insHisHis) | |
7 | g.55181301_55181302insCATCAC | CA176007 | EGFR,EGFR-AS1 | c.2133_2134insCATCAC (p.Tyr711_Val712insHisHis) c.641_642insCATCAC c.2292_2293insCATCAC (p.Tyr764_Val765insHisHis) c.*28+8373_*28+8374insCATCAC (n.*28+8373_*28+8374insCATCAC) c.2157_2158insCATCAC (p.Tyr719_Val720insHisHis) n.1271_1272insGATGGT c.1491_1492insCATCAC (p.Tyr497_Val498insHisHis) | ClinVar dbSNP |
7 | g.55181301C>A | CA367578532 | EGFR,EGFR-AS1 | c.2133C>A (p.Tyr711Ter) c.641C>A c.2292C>A (p.Tyr764Ter) c.*28+8373C>A (n.*28+8373C>A) c.2157C>A (p.Tyr719Ter) n.1270G>T c.1491C>A (p.Tyr497Ter) | |
7 | g.55181301C= | CA1708904964 | EGFR,EGFR-AS1 | c.2133C= (p.Tyr711=) c.641C= c.2292C= (p.Tyr764=) c.*28+8373C= (n.*28+8373C=) c.2157C= (p.Tyr719=) n.1270G= c.1491C= (p.Tyr497=) | |
7 | g.55181301C>G | CA367578533 | EGFR,EGFR-AS1 | c.2133C>G (p.Tyr711Ter) c.641C>G c.2292C>G (p.Tyr764Ter) c.*28+8373C>G (n.*28+8373C>G) c.2157C>G (p.Tyr719Ter) n.1270G>C c.1491C>G (p.Tyr497Ter) | dbSNP |
7 | g.55181301C>T | CA4266047 | EGFR,EGFR-AS1 | c.2133C>T (p.Tyr711=) c.641C>T c.2292C>T (p.Tyr764=) c.*28+8373C>T (n.*28+8373C>T) c.2157C>T (p.Tyr719=) n.1270G>A c.1491C>T (p.Tyr497=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
7 | g.55181302G>A | CA4266048 | EGFR,EGFR-AS1 | c.2134G>A (p.Val712Met) c.642G>A c.2293G>A (p.Val765Met) c.*28+8374G>A (n.*28+8374G>A) c.2158G>A (p.Val720Met) n.1269C>T c.1492G>A (p.Val498Met) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
7 | g.55181302G>C | CA4266049 | EGFR,EGFR-AS1 | c.2134G>C (p.Val712Leu) c.642G>C c.2293G>C (p.Val765Leu) c.*28+8374G>C (n.*28+8374G>C) c.2158G>C (p.Val720Leu) n.1269C>G c.1492G>C (p.Val498Leu) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.55181302G= | CA1708904980 | EGFR,EGFR-AS1 | c.2134G= (p.Val712=) c.642G= c.2293G= (p.Val765=) c.*28+8374G= (n.*28+8374G=) c.2158G= (p.Val720=) n.1269C= c.1492G= (p.Val498=) | |
7 | g.55181302G>T | CA367578538 | EGFR,EGFR-AS1 | c.2134G>T (p.Val712Leu) c.642G>T c.2293G>T (p.Val765Leu) c.*28+8374G>T (n.*28+8374G>T) c.2158G>T (p.Val720Leu) n.1269C>A c.1492G>T (p.Val498Leu) | ClinVar dbSNP gnomAD v4 |
7 | g.55181303T>A | CA367578541 | EGFR,EGFR-AS1 | c.2135T>A (p.Val712Glu) c.643T>A c.2294T>A (p.Val765Glu) c.*28+8375T>A (n.*28+8375T>A) c.2159T>A (p.Val720Glu) n.1268A>T c.1493T>A (p.Val498Glu) | dbSNP |
7 | g.55181303T>C | CA367578544 | EGFR,EGFR-AS1 | c.2135T>C (p.Val712Ala) c.643T>C c.2294T>C (p.Val765Ala) c.*28+8375T>C (n.*28+8375T>C) c.2159T>C (p.Val720Ala) n.1268A>G c.1493T>C (p.Val498Ala) | |
7 | g.55181303T>G | CA367578543 | EGFR,EGFR-AS1 | c.2135T>G (p.Val712Gly) c.643T>G c.2294T>G (p.Val765Gly) c.*28+8375T>G (n.*28+8375T>G) c.2159T>G (p.Val720Gly) n.1268A>C c.1493T>G (p.Val498Gly) | dbSNP COSMIC |
7 | g.55181304G>A | CA455165076 | EGFR,EGFR-AS1 | c.2136G>A (p.Val712=) c.644G>A c.2295G>A (p.Val765=) c.*28+8376G>A (n.*28+8376G>A) c.2160G>A (p.Val720=) n.1267C>T c.1494G>A (p.Val498=) | dbSNP |
7 | g.55181304G>C | CA455165078 | EGFR,EGFR-AS1 | c.2136G>C (p.Val712=) c.644G>C c.2295G>C (p.Val765=) c.*28+8376G>C (n.*28+8376G>C) c.2160G>C (p.Val720=) n.1267C>G c.1494G>C (p.Val498=) | ClinVar dbSNP |
7 | g.55181304G>T | CA455165077 | EGFR,EGFR-AS1 | c.2136G>T (p.Val712=) c.644G>T c.2295G>T (p.Val765=) c.*28+8376G>T (n.*28+8376G>T) c.2160G>T (p.Val720=) n.1267C>A c.1494G>T (p.Val498=) | |
7 | g.55181305A= | CA1708904986 | EGFR,EGFR-AS1 | c.2137A= (p.Met713=) c.645A= c.2296A= (p.Met766=) c.*28+8377A= (n.*28+8377A=) c.2161A= (p.Met721=) n.1266T= c.1495A= (p.Met499=) | |
7 | g.55181305A>C | CA367578547 | EGFR,EGFR-AS1 | c.2137A>C (p.Met713Leu) c.645A>C c.2296A>C (p.Met766Leu) c.*28+8377A>C (n.*28+8377A>C) c.2161A>C (p.Met721Leu) n.1266T>G c.1495A>C (p.Met499Leu) | dbSNP |
7 | g.55181305A>G | CA367578551 | EGFR,EGFR-AS1 | c.2137A>G (p.Met713Val) c.645A>G c.2296A>G (p.Met766Val) c.*28+8377A>G (n.*28+8377A>G) c.2161A>G (p.Met721Val) n.1266T>C c.1495A>G (p.Met499Val) | |
7 | g.55181305A>T | CA367578549 | EGFR,EGFR-AS1 | c.2137A>T (p.Met713Leu) c.645A>T c.2296A>T (p.Met766Leu) c.*28+8377A>T (n.*28+8377A>T) c.2161A>T (p.Met721Leu) n.1266T>A c.1495A>T (p.Met499Leu) | dbSNP gnomAD v2 gnomAD v4 |
7 | g.55181305_55181306delinsCA | CA2573102930 | EGFR,EGFR-AS1 | c.2137_2138delinsCA (p.Met713Gln) c.645_646delinsCA c.2296_2297delinsCA (p.Met766Gln) c.*28+8377_*28+8378delinsCA (n.*28+8377_*28+8378delinsCA) c.2161_2162delinsCA (p.Met721Gln) n.1265_1266delinsTG c.1495_1496delinsCA (p.Met499Gln) | |
7 | g.55181305_55181318dup | CA645561557 | EGFR,EGFR-AS1 | c.2137_2150dup (p.Asp717GlufsTer?) c.645_658dup c.2296_2309dup (p.Asp770GlufsTer?) c.*28+8377_*28+8390dup (n.*28+8377_*28+8390dup) c.2161_2174dup (p.Asp725GlufsTer?) n.1253_1266dup c.1495_1508dup (p.Asp503GlufsTer?) | COSMIC |
7 | g.55181306T>A | CA367578555 | EGFR,EGFR-AS1 | c.2138T>A (p.Met713Lys) c.646T>A c.2297T>A (p.Met766Lys) c.*28+8378T>A (n.*28+8378T>A) c.2162T>A (p.Met721Lys) n.1265A>T c.1496T>A (p.Met499Lys) | dbSNP |
7 | g.55181306T>C | CA367578561 | EGFR,EGFR-AS1 | c.2138T>C (p.Met713Thr) c.646T>C c.2297T>C (p.Met766Thr) c.*28+8378T>C (n.*28+8378T>C) c.2162T>C (p.Met721Thr) n.1265A>G c.1496T>C (p.Met499Thr) | COSMIC |
7 | g.55181306T>G | CA367578563 | EGFR,EGFR-AS1 | c.2138T>G (p.Met713Arg) c.646T>G c.2297T>G (p.Met766Arg) c.*28+8378T>G (n.*28+8378T>G) c.2162T>G (p.Met721Arg) n.1265A>C c.1496T>G (p.Met499Arg) | |
7 | g.55181311_55181312insCGCTGGCCA | CA645561559 | EGFR,EGFR-AS1 | c.2143_2144insCGCTGGCCA (p.Ala714_Ser715insThrLeuAla) c.651_652insCGCTGGCCA c.2302_2303insCGCTGGCCA (p.Ala767_Ser768insThrLeuAla) c.*28+8383_*28+8384insCGCTGGCCA (n.*28+8383_*28+8384insCGCTGGCCA) c.2167_2168insCGCTGGCCA (p.Ala722_Ser723insThrLeuAla) n.1265_1266insGCGTGGCCA c.1501_1502insCGCTGGCCA (p.Ala500_Ser501insThrLeuAla) | dbSNP COSMIC |
7 | g.55181312_55181313insTGTGGCCAG | CA645561558 | EGFR,EGFR-AS1 | c.2144_2145insTGTGGCCAG (p.Ser715_Val716insValAlaSer) c.652_653insTGTGGCCAG c.2303_2304insTGTGGCCAG (p.Ser768_Val769insValAlaSer) c.*28+8384_*28+8385insTGTGGCCAG (n.*28+8384_*28+8385insTGTGGCCAG) c.2168_2169insTGTGGCCAG (p.Ser723_Val724insValAlaSer) n.1265_1266insCACTGGCCA c.1502_1503insTGTGGCCAG (p.Ser501_Val502insValAlaSer) | dbSNP COSMIC |
7 | g.55181309_55181317dup | CA180588 | EGFR,EGFR-AS1 | c.2141_2149dup (p.Val716_Asp717insAlaSerVal) c.649_657dup c.2300_2308dup (p.Val769_Asp770insAlaSerVal) c.*28+8381_*28+8389dup (n.*28+8381_*28+8389dup) c.2165_2173dup (p.Val724_Asp725insAlaSerVal) n.1257_1265dup c.1499_1507dup (p.Val502_Asp503insAlaSerVal) | ClinVar dbSNP gnomAD v3 gnomAD v4 COSMIC COSMIC |
7 | g.55181307G>A | CA367578567 | EGFR,EGFR-AS1 | c.2139G>A (p.Met713Ile) c.647G>A c.2298G>A (p.Met766Ile) c.*28+8379G>A (n.*28+8379G>A) c.2163G>A (p.Met721Ile) n.1264C>T c.1497G>A (p.Met499Ile) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
7 | g.55181307G>C | CA367578566 | EGFR,EGFR-AS1 | c.2139G>C (p.Met713Ile) c.647G>C c.2298G>C (p.Met766Ile) c.*28+8379G>C (n.*28+8379G>C) c.2163G>C (p.Met721Ile) n.1264C>G c.1497G>C (p.Met499Ile) | dbSNP |
7 | g.55181307G= | CA1708904997 | EGFR,EGFR-AS1 | c.2139G= (p.Met713=) c.647G= c.2298G= (p.Met766=) c.*28+8379G= (n.*28+8379G=) c.2163G= (p.Met721=) n.1264C= c.1497G= (p.Met499=) | |
7 | g.55181307G>T | CA367578570 | EGFR,EGFR-AS1 | c.2139G>T (p.Met713Ile) c.647G>T c.2298G>T (p.Met766Ile) c.*28+8379G>T (n.*28+8379G>T) c.2163G>T (p.Met721Ile) n.1264C>A c.1497G>T (p.Met499Ile) | dbSNP |
7 | g.55181308G>A | CA367578576 | EGFR,EGFR-AS1 | c.2140G>A (p.Ala714Thr) c.648G>A c.2299G>A (p.Ala767Thr) c.*28+8380G>A (n.*28+8380G>A) c.2164G>A (p.Ala722Thr) n.1263C>T c.1498G>A (p.Ala500Thr) | |
7 | g.55181308G>C | CA367578574 | EGFR,EGFR-AS1 | c.2140G>C (p.Ala714Pro) c.648G>C c.2299G>C (p.Ala767Pro) c.*28+8380G>C (n.*28+8380G>C) c.2164G>C (p.Ala722Pro) n.1263C>G c.1498G>C (p.Ala500Pro) | |
7 | g.55181308G= | CA1708905002 | EGFR,EGFR-AS1 | c.2140G= (p.Ala714=) c.648G= c.2299G= (p.Ala767=) c.*28+8380G= (n.*28+8380G=) c.2164G= (p.Ala722=) n.1263C= c.1498G= (p.Ala500=) | |
7 | g.55181308G>T | CA158928267 | EGFR,EGFR-AS1 | c.2140G>T (p.Ala714Ser) c.648G>T c.2299G>T (p.Ala767Ser) c.*28+8380G>T (n.*28+8380G>T) c.2164G>T (p.Ala722Ser) n.1263C>A c.1498G>T (p.Ala500Ser) | ClinVar dbSNP gnomAD v4 |
7 | g.55181311_55181312insTAGCCA | CA645561560 | EGFR,EGFR-AS1 | c.2143_2144insTAGCCA (p.Ala714_Ser715insIleAla) c.651_652insTAGCCA c.2302_2303insTAGCCA (p.Ala767_Ser768insIleAla) c.*28+8383_*28+8384insTAGCCA (n.*28+8383_*28+8384insTAGCCA) c.2167_2168insTAGCCA (p.Ala722_Ser723insIleAla) n.1263_1264insTATGGC c.1501_1502insTAGCCA (p.Ala500_Ser501insIleAla) | dbSNP COSMIC |
7 | g.55181311_55181338del | CA2838010099 | EGFR,EGFR-AS1 | c.2143_2170del (p.Ser715CysfsTer?) c.651_678del c.2302_2329del (p.Ser768CysfsTer?) c.*28+8383_*28+8410del (n.*28+8383_*28+8410del) c.2167_2194del (p.Ser723CysfsTer?) n.1236_1263del c.1501_1528del (p.Ser501CysfsTer?) | |
7 | g.55181309C>A | CA367578581 | EGFR,EGFR-AS1 | c.2141C>A (p.Ala714Asp) c.649C>A c.2300C>A (p.Ala767Asp) c.*28+8381C>A (n.*28+8381C>A) c.2165C>A (p.Ala722Asp) n.1262G>T c.1499C>A (p.Ala500Asp) | dbSNP |
7 | g.55181309C= | CA1708905016 | EGFR,EGFR-AS1 | c.2141C= (p.Ala714=) c.649C= c.2300C= (p.Ala767=) c.*28+8381C= (n.*28+8381C=) c.2165C= (p.Ala722=) n.1262G= c.1499C= (p.Ala500=) | |
7 | g.55181309C>G | CA367578579 | EGFR,EGFR-AS1 | c.2141C>G (p.Ala714Gly) c.649C>G c.2300C>G (p.Ala767Gly) c.*28+8381C>G (n.*28+8381C>G) c.2165C>G (p.Ala722Gly) n.1262G>C c.1499C>G (p.Ala500Gly) | dbSNP |
7 | g.55181309C>T | CA135837 | EGFR,EGFR-AS1 | c.2141C>T (p.Ala714Val) c.649C>T c.2300C>T (p.Ala767Val) c.*28+8381C>T (n.*28+8381C>T) c.2165C>T (p.Ala722Val) n.1262G>A c.1499C>T (p.Ala500Val) | ClinVar dbSNP COSMIC |
7 | g.55181310C>A | CA455165081 | EGFR,EGFR-AS1 | c.2142C>A (p.Ala714=) c.650C>A c.2301C>A (p.Ala767=) c.*28+8382C>A (n.*28+8382C>A) c.2166C>A (p.Ala722=) n.1261G>T c.1500C>A (p.Ala500=) | |
7 | g.55181310C>G | CA455165079 | EGFR,EGFR-AS1 | c.2142C>G (p.Ala714=) c.650C>G c.2301C>G (p.Ala767=) c.*28+8382C>G (n.*28+8382C>G) c.2166C>G (p.Ala722=) n.1261G>C c.1500C>G (p.Ala500=) | dbSNP |
7 | g.55181310C>T | CA455165080 | EGFR,EGFR-AS1 | c.2142C>T (p.Ala714=) c.650C>T c.2301C>T (p.Ala767=) c.*28+8382C>T (n.*28+8382C>T) c.2166C>T (p.Ala722=) n.1261G>A c.1500C>T (p.Ala500=) | dbSNP |
7 | g.55181310_55181311delinsGG | CA645561562 | EGFR,EGFR-AS1 | c.2142_2143delinsGG (p.Ser715Gly) c.650_651delinsGG c.2301_2302delinsGG (p.Ser768Gly) c.*28+8382_*28+8383delinsGG (n.*28+8382_*28+8383delinsGG) c.2166_2167delinsGG (p.Ser723Gly) n.1260_1261delinsCC c.1500_1501delinsGG (p.Ser501Gly) | COSMIC |
7 | g.55181317_55181318insGCAGCGTGG | CA645561561 | EGFR,EGFR-AS1 | c.2149_2150insGCAGCGTGG (p.Val716_Asp717insGlySerVal) c.657_658insGCAGCGTGG c.2308_2309insGCAGCGTGG (p.Val769_Asp770insGlySerVal) c.*28+8389_*28+8390insGCAGCGTGG (n.*28+8389_*28+8390insGCAGCGTGG) c.2173_2174insGCAGCGTGG (p.Val724_Asp725insGlySerVal) n.1261_1262insCCCACGCTG c.1507_1508insGCAGCGTGG (p.Val502_Asp503insGlySerVal) | dbSNP COSMIC |
7 | g.55181312_55181320dup | CA135844 | EGFR,EGFR-AS1 | c.2144_2152dup (p.Asp717_Asn718insSerValAsp) c.652_660dup c.2303_2311dup (p.Asp770_Asn771insSerValAsp) c.*28+8384_*28+8392dup (n.*28+8384_*28+8392dup) c.2168_2176dup (p.Asp725_Asn726insSerValAsp) n.1253_1261dup c.1502_1510dup (p.Asp503_Asn504insSerValAsp) | ClinVar dbSNP COSMIC COSMIC COSMIC |
7 | g.55181310_55181311insTACGTGATG | CA645561563 | EGFR,EGFR-AS1 | c.2142_2143insTACGTGATG (p.Ala714_Ser715insTyrValMet) c.650_651insTACGTGATG c.2301_2302insTACGTGATG (p.Ala767_Ser768insTyrValMet) c.*28+8382_*28+8383insTACGTGATG (n.*28+8382_*28+8383insTACGTGATG) c.2166_2167insTACGTGATG (p.Ala722_Ser723insTyrValMet) n.1260_1261insCATCACGTA c.1500_1501insTACGTGATG (p.Ala500_Ser501insTyrValMet) | dbSNP COSMIC |
7 | g.55181311A= | CA1708905042 | EGFR,EGFR-AS1 | c.2143A= (p.Ser715=) c.651A= c.2302A= (p.Ser768=) c.*28+8383A= (n.*28+8383A=) c.2167A= (p.Ser723=) n.1260T= c.1501A= (p.Ser501=) | |
7 | g.55181311A>C | CA367578588 | EGFR,EGFR-AS1 | c.2143A>C (p.Ser715Arg) c.651A>C c.2302A>C (p.Ser768Arg) c.*28+8383A>C (n.*28+8383A>C) c.2167A>C (p.Ser723Arg) n.1260T>G c.1501A>C (p.Ser501Arg) | |
7 | g.55181311A>G | CA4266050 | EGFR,EGFR-AS1 | c.2143A>G (p.Ser715Gly) c.651A>G c.2302A>G (p.Ser768Gly) c.*28+8383A>G (n.*28+8383A>G) c.2167A>G (p.Ser723Gly) n.1260T>C c.1501A>G (p.Ser501Gly) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.55181311A>T | CA367578591 | EGFR,EGFR-AS1 | c.2143A>T (p.Ser715Cys) c.651A>T c.2302A>T (p.Ser768Cys) c.*28+8383A>T (n.*28+8383A>T) c.2167A>T (p.Ser723Cys) n.1260T>A c.1501A>T (p.Ser501Cys) | dbSNP |
7 | g.55181311_55181314delinsCCGC | CA891842006 | EGFR,EGFR-AS1 | c.2143_2146delinsCCGC (p.Ser715_Val716delinsProLeu) c.651_654delinsCCGC c.2302_2305delinsCCGC (p.Ser768_Val769delinsProLeu) c.*28+8383_*28+8386delinsCCGC (n.*28+8383_*28+8386delinsCCGC) c.2167_2170delinsCCGC (p.Ser723_Val724delinsProLeu) n.1257_1260delinsGCGG c.1501_1504delinsCCGC (p.Ser501_Val502delinsProLeu) | |
7 | g.55181317_55181318insGGAGCGTGG | CA645561564 | EGFR,EGFR-AS1 | c.2149_2150insGGAGCGTGG (p.Val716_Asp717insGlySerVal) c.657_658insGGAGCGTGG c.2308_2309insGGAGCGTGG (p.Val769_Asp770insGlySerVal) c.*28+8389_*28+8390insGGAGCGTGG (n.*28+8389_*28+8390insGGAGCGTGG) c.2173_2174insGGAGCGTGG (p.Val724_Asp725insGlySerVal) n.1260_1261insCCCCACGCT c.1507_1508insGGAGCGTGG (p.Val502_Asp503insGlySerVal) | dbSNP COSMIC |
7 | g.55181317_55181318insGTAGCGTGG | CA2573129744 | EGFR,EGFR-AS1 | c.2149_2150insGTAGCGTGG (p.Val716_Asp717insGlySerVal) c.657_658insGTAGCGTGG c.2308_2309insGTAGCGTGG (p.Val769_Asp770insGlySerVal) c.*28+8389_*28+8390insGTAGCGTGG (n.*28+8389_*28+8390insGTAGCGTGG) c.2173_2174insGTAGCGTGG (p.Val724_Asp725insGlySerVal) n.1260_1261insACCCACGCT c.1507_1508insGTAGCGTGG (p.Val502_Asp503insGlySerVal) | |
7 | g.55181312G>A | CA367578594 | EGFR,EGFR-AS1 | c.2144G>A (p.Ser715Asn) c.652G>A c.2303G>A (p.Ser768Asn) c.*28+8384G>A (n.*28+8384G>A) c.2168G>A (p.Ser723Asn) n.1259C>T c.1502G>A (p.Ser501Asn) | ClinVar dbSNP COSMIC |
7 | g.55181312G>C | CA367578596 | EGFR,EGFR-AS1 | c.2144G>C (p.Ser715Thr) c.652G>C c.2303G>C (p.Ser768Thr) c.*28+8384G>C (n.*28+8384G>C) c.2168G>C (p.Ser723Thr) n.1259C>G c.1502G>C (p.Ser501Thr) | dbSNP COSMIC |
7 | g.55181312G= | CA1708905063 | EGFR,EGFR-AS1 | c.2144G= (p.Ser715=) c.652G= c.2303G= (p.Ser768=) c.*28+8384G= (n.*28+8384G=) c.2168G= (p.Ser723=) n.1259C= c.1502G= (p.Ser501=) | |
7 | g.55181312G>T | CA135840 | EGFR,EGFR-AS1 | c.2144G>T (p.Ser715Ile) c.652G>T c.2303G>T (p.Ser768Ile) c.*28+8384G>T (n.*28+8384G>T) c.2168G>T (p.Ser723Ile) n.1259C>A c.1502G>T (p.Ser501Ile) | ClinVar dbSNP COSMIC |
7 | g.55181312_55181313delinsGC | CA1708905076 | EGFR,EGFR-AS1 | c.2144_2145delinsGC (p.Ser715=) c.652_653delinsGC c.2303_2304delinsGC (p.Ser768=) c.*28+8384_*28+8385delinsGC (n.*28+8384_*28+8385delinsGC) c.2168_2169delinsGC (p.Ser723=) n.1258_1259delinsGC c.1502_1503delinsGC (p.Ser501=) | |
7 | g.55181312_55181313delinsTT | CA135843 | EGFR,EGFR-AS1 | c.2144_2145delinsTT (p.Ser715Ile) c.652_653delinsTT c.2303_2304delinsTT (p.Ser768Ile) c.*28+8384_*28+8385delinsTT (n.*28+8384_*28+8385delinsTT) c.2168_2169delinsTT (p.Ser723Ile) n.1258_1259delinsAA c.1502_1503delinsTT (p.Ser501Ile) | ClinVar dbSNP |
7 | g.55181312_55181314delinsGCG | CA1708905072 | EGFR,EGFR-AS1 | c.2144_2146delinsGCG (p.Ser715=) c.652_654delinsGCG c.2303_2305delinsGCG (p.Ser768=) c.*28+8384_*28+8386delinsGCG (n.*28+8384_*28+8386delinsGCG) c.2168_2170delinsGCG (p.Ser723=) n.1257_1259delinsCGC c.1502_1504delinsGCG (p.Ser501=) | |
7 | g.55181312_55181314delinsTCC | CA2580617381 | EGFR,EGFR-AS1 | c.2144_2146delinsTCC (p.Ser715_Val716delinsIleLeu) c.652_654delinsTCC c.2303_2305delinsTCC (p.Ser768_Val769delinsIleLeu) c.*28+8384_*28+8386delinsTCC (n.*28+8384_*28+8386delinsTCC) c.2168_2170delinsTCC (p.Ser723_Val724delinsIleLeu) n.1257_1259delinsGGA c.1502_1504delinsTCC (p.Ser501_Val502delinsIleLeu) | |
7 | g.55181312_55181314delinsTCT | CA645561565 | EGFR,EGFR-AS1 | c.2144_2146delinsTCT (p.Ser715_Val716delinsIleLeu) c.652_654delinsTCT c.2303_2305delinsTCT (p.Ser768_Val769delinsIleLeu) c.*28+8384_*28+8386delinsTCT (n.*28+8384_*28+8386delinsTCT) c.2168_2170delinsTCT (p.Ser723_Val724delinsIleLeu) n.1257_1259delinsAGA c.1502_1504delinsTCT (p.Ser501_Val502delinsIleLeu) | ClinVar dbSNP COSMIC |
7 | g.55181316_55181317insTGCGTG | CA645561566 | EGFR,EGFR-AS1 | c.2148_2149insTGCGTG (p.Val716_Asp717insCysVal) c.656_657insTGCGTG c.2307_2308insTGCGTG (p.Val769_Asp770insCysVal) c.*28+8388_*28+8389insTGCGTG (n.*28+8388_*28+8389insTGCGTG) c.2172_2173insTGCGTG (p.Val724_Asp725insCysVal) n.1259_1260insACACGC c.1506_1507insTGCGTG (p.Val502_Asp503insCysVal) | dbSNP COSMIC |
7 | g.55181312_55181313insGCGTGGACA | CA158928300 | EGFR,EGFR-AS1 | c.2144_2145insGCGTGGACA (p.Ser715delinsArgArgGlyHis) c.652_653insGCGTGGACA c.2303_2304insGCGTGGACA (p.Ser768delinsArgArgGlyHis) c.*28+8384_*28+8385insGCGTGGACA (n.*28+8384_*28+8385insGCGTGGACA) c.2168_2169insGCGTGGACA (p.Ser723delinsArgArgGlyHis) n.1258_1259insTGTCCACGC c.1502_1503insGCGTGGACA (p.Ser501delinsArgArgGlyHis) | dbSNP |
7 | g.55181312_55181313insTGTGGCCAA | CA645561569 | EGFR,EGFR-AS1 | c.2144_2145insTGTGGCCAA (p.Ser715_Val716insValAlaAsn) c.652_653insTGTGGCCAA c.2303_2304insTGTGGCCAA (p.Ser768_Val769insValAlaAsn) c.*28+8384_*28+8385insTGTGGCCAA (n.*28+8384_*28+8385insTGTGGCCAA) c.2168_2169insTGTGGCCAA (p.Ser723_Val724insValAlaAsn) n.1258_1259insTTGGCCACA c.1502_1503insTGTGGCCAA (p.Ser501_Val502insValAlaAsn) | dbSNP COSMIC |
7 | g.55181313C>A | CA367578606 | EGFR,EGFR-AS1 | c.2145C>A (p.Ser715Arg) c.653C>A c.2304C>A (p.Ser768Arg) c.*28+8385C>A (n.*28+8385C>A) c.2169C>A (p.Ser723Arg) n.1258G>T c.1503C>A (p.Ser501Arg) | ClinVar dbSNP |
7 | g.55181313C= | CA1708905098 | EGFR,EGFR-AS1 | c.2145C= (p.Ser715=) c.653C= c.2304C= (p.Ser768=) c.*28+8385C= (n.*28+8385C=) c.2169C= (p.Ser723=) n.1258G= c.1503C= (p.Ser501=) | |
7 | g.55181313C>G | CA367578605 | EGFR,EGFR-AS1 | c.2145C>G (p.Ser715Arg) c.653C>G c.2304C>G (p.Ser768Arg) c.*28+8385C>G (n.*28+8385C>G) c.2169C>G (p.Ser723Arg) n.1258G>C c.1503C>G (p.Ser501Arg) | dbSNP gnomAD v2 |
7 | g.55181313C>T | CA4266051 | EGFR,EGFR-AS1 | c.2145C>T (p.Ser715=) c.653C>T c.2304C>T (p.Ser768=) c.*28+8385C>T (n.*28+8385C>T) c.2169C>T (p.Ser723=) n.1258G>A c.1503C>T (p.Ser501=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.55181317_55181318insGGGTCGTGG | CA645561568 | EGFR,EGFR-AS1 | c.2149_2150insGGGTCGTGG (p.Val716_Asp717insGlyValVal) c.657_658insGGGTCGTGG c.2308_2309insGGGTCGTGG (p.Val769_Asp770insGlyValVal) c.*28+8389_*28+8390insGGGTCGTGG (n.*28+8389_*28+8390insGGGTCGTGG) c.2173_2174insGGGTCGTGG (p.Val724_Asp725insGlyValVal) n.1258_1259insACCCCCACG c.1507_1508insGGGTCGTGG (p.Val502_Asp503insGlyValVal) | dbSNP COSMIC |
7 | g.55181314_55181322dup | CA645561567 | EGFR,EGFR-AS1 | c.2146_2154dup (p.Asn718_Pro719insValAspAsn) c.654_662dup c.2305_2313dup (p.Asn771_Pro772insValAspAsn) c.*28+8386_*28+8394dup (n.*28+8386_*28+8394dup) c.2170_2178dup (p.Asn726_Pro727insValAspAsn) n.1250_1258dup c.1504_1512dup (p.Asn504_Pro505insValAspAsn) | dbSNP COSMIC |
7 | g.55181317_55181331dup | CA181058 | EGFR,EGFR-AS1 | c.2149_2163dup (p.Val721_Cys722insAspAsnProHisVal) c.657_671dup c.2308_2322dup (p.Val774_Cys775insAspAsnProHisVal) c.*28+8389_*28+8403dup (n.*28+8389_*28+8403dup) c.2173_2187dup (p.Val729_Cys730insAspAsnProHisVal) n.1244_1258dup c.1507_1521dup (p.Val507_Cys508insAspAsnProHisVal) | ClinVar dbSNP |
7 | g.55181314G>A | CA350947 | EGFR,EGFR-AS1 | c.2146G>A (p.Val716Met) c.654G>A c.2305G>A (p.Val769Met) c.*28+8386G>A (n.*28+8386G>A) c.2170G>A (p.Val724Met) n.1257C>T c.1504G>A (p.Val502Met) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
7 | g.55181314G>C | CA135847 | EGFR,EGFR-AS1 | c.2146G>C (p.Val716Leu) c.654G>C c.2305G>C (p.Val769Leu) c.*28+8386G>C (n.*28+8386G>C) c.2170G>C (p.Val724Leu) n.1257C>G c.1504G>C (p.Val502Leu) | ClinVar dbSNP |
7 | g.55181314G= | CA1708905112 | EGFR,EGFR-AS1 | c.2146G= (p.Val716=) c.654G= c.2305G= (p.Val769=) c.*28+8386G= (n.*28+8386G=) c.2170G= (p.Val724=) n.1257C= c.1504G= (p.Val502=) | |
7 | g.55181314G>T | CA135850 | EGFR,EGFR-AS1 | c.2146G>T (p.Val716Leu) c.654G>T c.2305G>T (p.Val769Leu) c.*28+8386G>T (n.*28+8386G>T) c.2170G>T (p.Val724Leu) n.1257C>A c.1504G>T (p.Val502Leu) | ClinVar dbSNP COSMIC |
7 | g.55181316_55181317insTGTGTG | CA2018007660 | EGFR,EGFR-AS1 | c.2148_2149insTGTGTG (p.Val716_Asp717insCysVal) c.656_657insTGTGTG c.2307_2308insTGTGTG (p.Val769_Asp770insCysVal) c.*28+8388_*28+8389insTGTGTG (n.*28+8388_*28+8389insTGTGTG) c.2172_2173insTGTGTG (p.Val724_Asp725insCysVal) n.1257_1258insACACAC c.1506_1507insTGTGTG (p.Val502_Asp503insCysVal) | |
7 | g.55181315_55181317dup | CA2714932002 | EGFR,EGFR-AS1 | c.2147_2149dup (p.Val716_Asp717insVal) c.655_657dup c.2306_2308dup (p.Val769_Asp770insVal) c.*28+8387_*28+8389dup (n.*28+8387_*28+8389dup) c.2171_2173dup (p.Val724_Asp725insVal) n.1255_1257dup c.1505_1507dup (p.Val502_Asp503insVal) | dbSNP |
7 | g.55181315T>A | CA367578615 | EGFR,EGFR-AS1 | c.2147T>A (p.Val716Glu) c.655T>A c.2306T>A (p.Val769Glu) c.*28+8387T>A (n.*28+8387T>A) c.2171T>A (p.Val724Glu) n.1256A>T c.1505T>A (p.Val502Glu) | |
7 | g.55181315T>C | CA367578616 | EGFR,EGFR-AS1 | c.2147T>C (p.Val716Ala) c.655T>C c.2306T>C (p.Val769Ala) c.*28+8387T>C (n.*28+8387T>C) c.2171T>C (p.Val724Ala) n.1256A>G c.1505T>C (p.Val502Ala) | ClinVar COSMIC |
7 | g.55181315T>G | CA367578618 | EGFR,EGFR-AS1 | c.2147T>G (p.Val716Gly) c.655T>G c.2306T>G (p.Val769Gly) c.*28+8387T>G (n.*28+8387T>G) c.2171T>G (p.Val724Gly) n.1256A>C c.1505T>G (p.Val502Gly) | |
7 | g.55181315T= | CA1708905123 | EGFR,EGFR-AS1 | c.2147T= (p.Val716=) c.655T= c.2306T= (p.Val769=) c.*28+8387T= (n.*28+8387T=) c.2171T= (p.Val724=) n.1256A= c.1505T= (p.Val502=) | |
7 | g.55181316G>A | CA4266052 | EGFR,EGFR-AS1 | c.2148G>A (p.Val716=) c.656G>A c.2307G>A (p.Val769=) c.*28+8388G>A (n.*28+8388G>A) c.2172G>A (p.Val724=) n.1255C>T c.1506G>A (p.Val502=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
7 | g.55181316G>C | CA455165083 | EGFR,EGFR-AS1 | c.2148G>C (p.Val716=) c.656G>C c.2307G>C (p.Val769=) c.*28+8388G>C (n.*28+8388G>C) c.2172G>C (p.Val724=) n.1255C>G c.1506G>C (p.Val502=) | |
7 | g.55181316G= | CA1708905135 | EGFR,EGFR-AS1 | c.2148G= (p.Val716=) c.656G= c.2307G= (p.Val769=) c.*28+8388G= (n.*28+8388G=) c.2172G= (p.Val724=) n.1255C= c.1506G= (p.Val502=) | |
7 | g.55181316G>T | CA455165082 | EGFR,EGFR-AS1 | c.2148G>T (p.Val716=) c.656G>T c.2307G>T (p.Val769=) c.*28+8388G>T (n.*28+8388G>T) c.2172G>T (p.Val724=) n.1255C>A c.1506G>T (p.Val502=) | dbSNP |
7 | g.55181316_55181319delinsGGAC | CA1708905134 | EGFR,EGFR-AS1 | c.2148_2151delinsGGAC (p.Val716=) c.656_659delinsGGAC c.2307_2310delinsGGAC (p.Val769=) c.*28+8388_*28+8391delinsGGAC (n.*28+8388_*28+8391delinsGGAC) c.2172_2175delinsGGAC (p.Val724=) n.1252_1255delinsGTCC c.1506_1509delinsGGAC (p.Val502=) | |
7 | g.55181319_55181320insGGGGAC | CA645561570 | EGFR,EGFR-AS1 | c.2151_2152insGGGGAC (p.Asp717_Asn718insGlyAsp) c.659_660insGGGGAC c.2310_2311insGGGGAC (p.Asp770_Asn771insGlyAsp) c.*28+8391_*28+8392insGGGGAC (n.*28+8391_*28+8392insGGGGAC) c.2175_2176insGGGGAC (p.Asp725_Asn726insGlyAsp) n.1255_1256insCCGTCC c.1509_1510insGGGGAC (p.Asp503_Asn504insGlyAsp) | dbSNP COSMIC |
7 | g.55181316_55181324dup | CA180579 | EGFR,EGFR-AS1 | c.2148_2156dup (p.Pro719_His720insAspAsnPro) c.656_664dup c.2307_2315dup (p.Pro772_His773insAspAsnPro) c.*28+8388_*28+8396dup (n.*28+8388_*28+8396dup) c.2172_2180dup (p.Pro727_His728insAspAsnPro) n.1247_1255dup c.1506_1514dup (p.Pro505_His506insAspAsnPro) | ClinVar dbSNP |
7 | g.55181316_55181317insATGGCCAGCGTGGAC | CA645561572 | EGFR,EGFR-AS1 | c.2148_2149insATGGCCAGCGTGGAC (p.Val716_Asp717insMetAlaSerValAsp) c.656_657insATGGCCAGCGTGGAC c.2307_2308insATGGCCAGCGTGGAC (p.Val769_Asp770insMetAlaSerValAsp) c.*28+8388_*28+8389insATGGCCAGCGTGGAC (n.*28+8388_*28+8389insATGGCCAGCGTGGAC) c.2172_2173insATGGCCAGCGTGGAC (p.Val724_Asp725insMetAlaSerValAsp) n.1254_1255insGTCCACGCTGGCCAT c.1506_1507insATGGCCAGCGTGGAC (p.Val502_Asp503insMetAlaSerValAsp) | dbSNP COSMIC |
7 | g.55181317G>A | CA367578627 | EGFR,EGFR-AS1 | c.2149G>A (p.Asp717Asn) c.657G>A c.2308G>A (p.Asp770Asn) c.*28+8389G>A (n.*28+8389G>A) c.2173G>A (p.Asp725Asn) n.1254C>T c.1507G>A (p.Asp503Asn) | ClinVar dbSNP COSMIC |
7 | g.55181317G>C | CA367578628 | EGFR,EGFR-AS1 | c.2149G>C (p.Asp717His) c.657G>C c.2308G>C (p.Asp770His) c.*28+8389G>C (n.*28+8389G>C) c.2173G>C (p.Asp725His) n.1254C>G c.1507G>C (p.Asp503His) | dbSNP |
7 | g.55181317G= | CA1708905145 | EGFR,EGFR-AS1 | c.2149G= (p.Asp717=) c.657G= c.2308G= (p.Asp770=) c.*28+8389G= (n.*28+8389G=) c.2173G= (p.Asp725=) n.1254C= c.1507G= (p.Asp503=) | |
7 | g.55181317G>T | CA367578624 | EGFR,EGFR-AS1 | c.2149G>T (p.Asp717Tyr) c.657G>T c.2308G>T (p.Asp770Tyr) c.*28+8389G>T (n.*28+8389G>T) c.2173G>T (p.Asp725Tyr) n.1254C>A c.1507G>T (p.Asp503Tyr) | dbSNP |
7 | g.55181318_55181319insGCGTGGAGA | CA645561574 | EGFR,EGFR-AS1 | c.2150_2151insGCGTGGAGA (p.Val716_Asp717insGluArgGly) c.658_659insGCGTGGAGA c.2309_2310insGCGTGGAGA (p.Val769_Asp770insGluArgGly) c.*28+8390_*28+8391insGCGTGGAGA (n.*28+8390_*28+8391insGCGTGGAGA) c.2174_2175insGCGTGGAGA (p.Val724_Asp725insGluArgGly) n.1254_1255insTCCACGCTC c.1508_1509insGCGTGGAGA (p.Val502_Asp503insGluArgGly) | dbSNP COSMIC |
7 | g.55181317_55181319delinsTGGG | CA176010 | EGFR,EGFR-AS1 | c.2149_2151delinsTGGG (p.Asp717TrpfsTer?) c.657_659delinsTGGG c.2308_2310delinsTGGG (p.Asp770TrpfsTer?) c.*28+8389_*28+8391delinsTGGG (n.*28+8389_*28+8391delinsTGGG) c.2173_2175delinsTGGG (p.Asp725TrpfsTer?) n.1252_1254delinsCCCA c.1507_1509delinsTGGG (p.Asp503TrpfsTer?) | ClinVar dbSNP |
7 | g.55181319_55181320insGGCGAC | CA645561573 | EGFR,EGFR-AS1 | c.2151_2152insGGCGAC (p.Asp717_Asn718insGlyAsp) c.659_660insGGCGAC c.2310_2311insGGCGAC (p.Asp770_Asn771insGlyAsp) c.*28+8391_*28+8392insGGCGAC (n.*28+8391_*28+8392insGGCGAC) c.2175_2176insGGCGAC (p.Asp725_Asn726insGlyAsp) n.1254_1255insGCCGTC c.1509_1510insGGCGAC (p.Asp503_Asn504insGlyAsp) | dbSNP COSMIC |
7 | g.55181317_55181324delinsCCAGCGTGGATAACCG | CA645561571 | EGFR,EGFR-AS1 | c.2149_2156delinsCCAGCGTGGATAACCG (p.Asp717ProfsTer?) c.657_664delinsCCAGCGTGGATAACCG c.2308_2315delinsCCAGCGTGGATAACCG (p.Asp770ProfsTer?) c.*28+8389_*28+8396delinsCCAGCGTGGATAACCG (n.*28+8389_*28+8396delinsCCAGCGTGGATAACCG) c.2173_2180delinsCCAGCGTGGATAACCG (p.Asp725ProfsTer?) n.1247_1254delinsCGGTTATCCACGCTGG c.1507_1514delinsCCAGCGTGGATAACCG (p.Asp503ProfsTer?) | COSMIC |
7 | g.55181317_55181325dup | CA645561575 | EGFR,EGFR-AS1 | c.2149_2157dup (p.Pro719_His720insAspAsnPro) c.657_665dup c.2308_2316dup (p.Pro772_His773insAspAsnPro) c.*28+8389_*28+8397dup (n.*28+8389_*28+8397dup) c.2173_2181dup (p.Pro727_His728insAspAsnPro) n.1246_1254dup c.1507_1515dup (p.Pro505_His506insAspAsnPro) | dbSNP COSMIC |
7 | g.55181317_55181318insGTT | CA180585 | EGFR,EGFR-AS1 | c.2149_2150insGTT (p.Asp717delinsGlyTyr) c.657_658insGTT c.2308_2309insGTT (p.Asp770delinsGlyTyr) c.*28+8389_*28+8390insGTT (n.*28+8389_*28+8390insGTT) c.2173_2174insGTT (p.Asp725delinsGlyTyr) n.1253_1254insAAC c.1507_1508insGTT (p.Asp503delinsGlyTyr) | ClinVar dbSNP COSMIC |
7 | g.55181318A= | CA1708905168 | EGFR,EGFR-AS1 | c.2150A= (p.Asp717=) c.658A= c.2309A= (p.Asp770=) c.*28+8390A= (n.*28+8390A=) c.2174A= (p.Asp725=) n.1253T= c.1508A= (p.Asp503=) | |
7 | g.55181318A>C | CA367578638 | EGFR,EGFR-AS1 | c.2150A>C (p.Asp717Ala) c.658A>C c.2309A>C (p.Asp770Ala) c.*28+8390A>C (n.*28+8390A>C) c.2174A>C (p.Asp725Ala) n.1253T>G c.1508A>C (p.Asp503Ala) | dbSNP |
7 | g.55181318A>G | CA367578640 | EGFR,EGFR-AS1 | c.2150A>G (p.Asp717Gly) c.658A>G c.2309A>G (p.Asp770Gly) c.*28+8390A>G (n.*28+8390A>G) c.2174A>G (p.Asp725Gly) n.1253T>C c.1508A>G (p.Asp503Gly) | dbSNP gnomAD v4 |
7 | g.55181318A>T | CA367578642 | EGFR,EGFR-AS1 | c.2150A>T (p.Asp717Val) c.658A>T c.2309A>T (p.Asp770Val) c.*28+8390A>T (n.*28+8390A>T) c.2174A>T (p.Asp725Val) n.1253T>A c.1508A>T (p.Asp503Val) | dbSNP |
7 | g.55181318_55181319delinsGCACG | CA2573051062 | EGFR,EGFR-AS1 | c.2150_2151delinsGCACG (p.Asp717delinsGlyThr) c.658_659delinsGCACG c.2309_2310delinsGCACG (p.Asp770delinsGlyThr) c.*28+8390_*28+8391delinsGCACG (n.*28+8390_*28+8391delinsGCACG) c.2174_2175delinsGCACG (p.Asp725delinsGlyThr) n.1252_1253delinsCGTGC c.1508_1509delinsGCACG (p.Asp503delinsGlyThr) | |
7 | g.55181318_55181319delinsCCAGCGTGGAT | CA645561579 | EGFR,EGFR-AS1 | c.2150_2151delinsCCAGCGTGGAT (p.Val716_Asp717insAlaSerVal) c.658_659delinsCCAGCGTGGAT c.2309_2310delinsCCAGCGTGGAT (p.Val769_Asp770insAlaSerVal) c.*28+8390_*28+8391delinsCCAGCGTGGAT (n.*28+8390_*28+8391delinsCCAGCGTGGAT) c.2174_2175delinsCCAGCGTGGAT (p.Val724_Asp725insAlaSerVal) n.1252_1253delinsATCCACGCTGG c.1508_1509delinsCCAGCGTGGAT (p.Val502_Asp503insAlaSerVal) | dbSNP COSMIC |
7 | g.55181319_55181320insTAC | CA645561577 | EGFR,EGFR-AS1 | c.2151_2152insTAC (p.Asp717_Asn718insTyr) c.659_660insTAC c.2310_2311insTAC (p.Asp770_Asn771insTyr) c.*28+8391_*28+8392insTAC (n.*28+8391_*28+8392insTAC) c.2175_2176insTAC (p.Asp725_Asn726insTyr) n.1253_1254insAGT c.1509_1510insTAC (p.Asp503_Asn504insTyr) | dbSNP COSMIC |
7 | g.55181318_55181321delinsCTGGTGG | CA645561578 | EGFR,EGFR-AS1 | c.2150_2153delinsCTGGTGG (p.Asp717_Asn718delinsAlaGlyGly) c.658_661delinsCTGGTGG c.2309_2312delinsCTGGTGG (p.Asp770_Asn771delinsAlaGlyGly) c.*28+8390_*28+8393delinsCTGGTGG (n.*28+8390_*28+8393delinsCTGGTGG) c.2174_2177delinsCTGGTGG (p.Asp725_Asn726delinsAlaGlyGly) n.1250_1253delinsCCACCAG c.1508_1511delinsCTGGTGG (p.Asp503_Asn504delinsAlaGlyGly) | dbSNP COSMIC |
7 | g.55181320_55181322dup | CA645561576 | EGFR,EGFR-AS1 | c.2152_2154dup (p.Asn718_Pro719insAsn) c.660_662dup c.2311_2313dup (p.Asn771_Pro772insAsn) c.*28+8392_*28+8394dup (n.*28+8392_*28+8394dup) c.2176_2178dup (p.Asn726_Pro727insAsn) n.1251_1253dup c.1510_1512dup (p.Asn504_Pro505insAsn) | dbSNP COSMIC COSMIC |
7 | g.55181320_55181328dup | CA180983 | EGFR,EGFR-AS1 | c.2152_2160dup (p.His720_Val721insAsnProHis) c.660_668dup c.2311_2319dup (p.His773_Val774insAsnProHis) c.*28+8392_*28+8400dup (n.*28+8392_*28+8400dup) c.2176_2184dup (p.His728_Val729insAsnProHis) n.1245_1253dup c.1510_1518dup (p.His506_Val507insAsnProHis) | ClinVar dbSNP COSMIC COSMIC |
7 | g.55181318_55181319insGTC | CA658795342 | EGFR,EGFR-AS1 | c.2150_2151insGTC (p.Asp717delinsGluSer) c.658_659insGTC c.2309_2310insGTC (p.Asp770delinsGluSer) c.*28+8390_*28+8391insGTC (n.*28+8390_*28+8391insGTC) c.2174_2175insGTC (p.Asp725delinsGluSer) n.1252_1253insGAC c.1508_1509insGTC (p.Asp503delinsGluSer) | ClinVar dbSNP |
7 | g.55181319C>A | CA367578648 | EGFR,EGFR-AS1 | c.2151C>A (p.Asp717Glu) c.659C>A c.2310C>A (p.Asp770Glu) c.*28+8391C>A (n.*28+8391C>A) c.2175C>A (p.Asp725Glu) n.1252G>T c.1509C>A (p.Asp503Glu) | ClinVar dbSNP |
7 | g.55181319C= | CA1708905179 | EGFR,EGFR-AS1 | c.2151C= (p.Asp717=) c.659C= c.2310C= (p.Asp770=) c.*28+8391C= (n.*28+8391C=) c.2175C= (p.Asp725=) n.1252G= c.1509C= (p.Asp503=) | |
7 | g.55181319C>G | CA367578646 | EGFR,EGFR-AS1 | c.2151C>G (p.Asp717Glu) c.659C>G c.2310C>G (p.Asp770Glu) c.*28+8391C>G (n.*28+8391C>G) c.2175C>G (p.Asp725Glu) n.1252G>C c.1509C>G (p.Asp503Glu) | |
7 | g.55181319C>T | CA135851 | EGFR,EGFR-AS1 | c.2151C>T (p.Asp717=) c.659C>T c.2310C>T (p.Asp770=) c.*28+8391C>T (n.*28+8391C>T) c.2175C>T (p.Asp725=) n.1252G>A c.1509C>T (p.Asp503=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
7 | g.55181319_55181320insGGC | CA645561584 | EGFR,EGFR-AS1 | c.2151_2152insGGC (p.Asp717_Asn718insGly) c.659_660insGGC c.2310_2311insGGC (p.Asp770_Asn771insGly) c.*28+8391_*28+8392insGGC (n.*28+8391_*28+8392insGGC) c.2175_2176insGGC (p.Asp725_Asn726insGly) n.1252_1253insCCG c.1509_1510insGGC (p.Asp503_Asn504insGly) | dbSNP COSMIC |
7 | g.55181319_55181320insCAGCGTGGC | CA645561583 | EGFR,EGFR-AS1 | c.2151_2152insCAGCGTGGC (p.Asp717_Asn718insGlnArgGly) c.659_660insCAGCGTGGC c.2310_2311insCAGCGTGGC (p.Asp770_Asn771insGlnArgGly) c.*28+8391_*28+8392insCAGCGTGGC (n.*28+8391_*28+8392insCAGCGTGGC) c.2175_2176insCAGCGTGGC (p.Asp725_Asn726insGlnArgGly) n.1252_1253insCCACGCTGG c.1509_1510insCAGCGTGGC (p.Asp503_Asn504insGlnArgGly) | dbSNP COSMIC |
7 | g.55181320_55181321insCCA | CA645561580 | EGFR,EGFR-AS1 | c.2152_2153insCCA (p.Asp717_Asn718insThr) c.660_661insCCA c.2311_2312insCCA (p.Asp770_Asn771insThr) c.*28+8392_*28+8393insCCA (n.*28+8392_*28+8393insCCA) c.2176_2177insCCA (p.Asp725_Asn726insThr) n.1252_1253insGTG c.1510_1511insCCA (p.Asp503_Asn504insThr) | dbSNP COSMIC |
7 | g.55181320_55181321insTGGCCACCCCCA | CA645561581 | EGFR,EGFR-AS1 | c.2152_2153insTGGCCACCCCCA (p.Asp717_Asn718insMetAlaThrPro) c.660_661insTGGCCACCCCCA c.2311_2312insTGGCCACCCCCA (p.Asp770_Asn771insMetAlaThrPro) c.*28+8392_*28+8393insTGGCCACCCCCA (n.*28+8392_*28+8393insTGGCCACCCCCA) c.2176_2177insTGGCCACCCCCA (p.Asp725_Asn726insMetAlaThrPro) n.1252_1253insGGGGTGGCCATG c.1510_1511insTGGCCACCCCCA (p.Asp503_Asn504insMetAlaThrPro) | dbSNP COSMIC |
7 | g.55181325_55181326insGGCAACCCC | CA2573051057 | EGFR,EGFR-AS1 | c.2157_2158insGGCAACCCC (p.Pro719_His720insGlyAsnPro) c.665_666insGGCAACCCC c.2316_2317insGGCAACCCC (p.Pro772_His773insGlyAsnPro) c.*28+8397_*28+8398insGGCAACCCC (n.*28+8397_*28+8398insGGCAACCCC) c.2181_2182insGGCAACCCC (p.Pro727_His728insGlyAsnPro) n.1252_1253insCCGGGGTTG c.1515_1516insGGCAACCCC (p.Pro505_His506insGlyAsnPro) | |
7 | g.55181320_55181325dup | CA2714932357 | EGFR,EGFR-AS1 | c.2152_2157dup (p.Pro719_His720insAsnPro) c.660_665dup c.2311_2316dup (p.Pro772_His773insAsnPro) c.*28+8392_*28+8397dup (n.*28+8392_*28+8397dup) c.2176_2181dup (p.Pro727_His728insAsnPro) n.1247_1252dup c.1510_1515dup (p.Pro505_His506insAsnPro) | dbSNP |
7 | g.55181329_55181330insGCAACCCCCACG | CA645561582 | EGFR,EGFR-AS1 | c.2161_2162insGCAACCCCCACG (p.His720_Val721insGlyAsnProHis) c.669_670insGCAACCCCCACG c.2320_2321insGCAACCCCCACG (p.His773_Val774insGlyAsnProHis) c.*28+8401_*28+8402insGCAACCCCCACG (n.*28+8401_*28+8402insGCAACCCCCACG) c.2185_2186insGCAACCCCCACG (p.His728_Val729insGlyAsnProHis) n.1252_1253insCCGTGGGGGTTG c.1519_1520insGCAACCCCCACG (p.His506_Val507insGlyAsnProHis) | dbSNP COSMIC |
7 | g.55181319_55181320insGGG | CA891842013 | EGFR,EGFR-AS1 | c.2151_2152insGGG (p.Asp717_Asn718insGly) c.659_660insGGG c.2310_2311insGGG (p.Asp770_Asn771insGly) c.*28+8391_*28+8392insGGG (n.*28+8391_*28+8392insGGG) c.2175_2176insGGG (p.Asp725_Asn726insGly) n.1251_1252insCCC c.1509_1510insGGG (p.Asp503_Asn504insGly) | |
7 | g.55181319_55181320insGGT | CA645561591 | EGFR,EGFR-AS1 | c.2151_2152insGGT (p.Asp717_Asn718insGly) c.659_660insGGT c.2310_2311insGGT (p.Asp770_Asn771insGly) c.*28+8391_*28+8392insGGT (n.*28+8391_*28+8392insGGT) c.2175_2176insGGT (p.Asp725_Asn726insGly) n.1251_1252insACC c.1509_1510insGGT (p.Asp503_Asn504insGly) | dbSNP COSMIC |
7 | g.55181319_55181320insGGCACA | CA645561586 | EGFR,EGFR-AS1 | c.2151_2152insGGCACA (p.Asp717_Asn718insGlyThr) c.659_660insGGCACA c.2310_2311insGGCACA (p.Asp770_Asn771insGlyThr) c.*28+8391_*28+8392insGGCACA (n.*28+8391_*28+8392insGGCACA) c.2175_2176insGGCACA (p.Asp725_Asn726insGlyThr) n.1251_1252insTGTGCC c.1509_1510insGGCACA (p.Asp503_Asn504insGlyThr) | dbSNP COSMIC |
7 | g.55181319_55181320insGGGTTA | CA645561585 | EGFR,EGFR-AS1 | c.2151_2152insGGGTTA (p.Asp717_Asn718insGlyLeu) c.659_660insGGGTTA c.2310_2311insGGGTTA (p.Asp770_Asn771insGlyLeu) c.*28+8391_*28+8392insGGGTTA (n.*28+8391_*28+8392insGGGTTA) c.2175_2176insGGGTTA (p.Asp725_Asn726insGlyLeu) n.1251_1252insTAACCC c.1509_1510insGGGTTA (p.Asp503_Asn504insGlyLeu) | dbSNP COSMIC |
7 | g.55181319_55181320insGGGTTG | CA135854 | EGFR,EGFR-AS1 | c.2151_2152insGGGTTG (p.Asp717_Asn718insGlyLeu) c.659_660insGGGTTG c.2310_2311insGGGTTG (p.Asp770_Asn771insGlyLeu) c.*28+8391_*28+8392insGGGTTG (n.*28+8391_*28+8392insGGGTTG) c.2175_2176insGGGTTG (p.Asp725_Asn726insGlyLeu) n.1251_1252insCAACCC c.1509_1510insGGGTTG (p.Asp503_Asn504insGlyLeu) | ClinVar dbSNP |
7 | g.55181319_55181320insGGGTTT | CA645561590 | EGFR,EGFR-AS1 | c.2151_2152insGGGTTT (p.Asp717_Asn718insGlyPhe) c.659_660insGGGTTT c.2310_2311insGGGTTT (p.Asp770_Asn771insGlyPhe) c.*28+8391_*28+8392insGGGTTT (n.*28+8391_*28+8392insGGGTTT) c.2175_2176insGGGTTT (p.Asp725_Asn726insGlyPhe) n.1251_1252insAAACCC c.1509_1510insGGGTTT (p.Asp503_Asn504insGlyPhe) | dbSNP COSMIC |
7 | g.55181319_55181320insGCACCGTGG | CA645561592 | EGFR,EGFR-AS1 | c.2151_2152insGCACCGTGG (p.Asp717_Asn718insAlaProTrp) c.659_660insGCACCGTGG c.2310_2311insGCACCGTGG (p.Asp770_Asn771insAlaProTrp) c.*28+8391_*28+8392insGCACCGTGG (n.*28+8391_*28+8392insGCACCGTGG) c.2175_2176insGCACCGTGG (p.Asp725_Asn726insAlaProTrp) n.1251_1252insCCACGGTGC c.1509_1510insGCACCGTGG (p.Asp503_Asn504insAlaProTrp) | dbSNP COSMIC |
7 | g.55181320A= | CA913203559 | EGFR,EGFR-AS1 | c.2152A= (p.Asn718=) c.660A= c.2311A= (p.Asn771=) c.*28+8392A= (n.*28+8392A=) c.2176A= (p.Asn726=) n.1251T= c.1510A= (p.Asn504=) | |
7 | g.55181320A>C | CA367578653 | EGFR,EGFR-AS1 | c.2152A>C (p.Asn718His) c.660A>C c.2311A>C (p.Asn771His) c.*28+8392A>C (n.*28+8392A>C) c.2176A>C (p.Asn726His) n.1251T>G c.1510A>C (p.Asn504His) | |
7 | g.55181320A>G | CA176014 | EGFR,EGFR-AS1 | c.2152A>G (p.Asn718Asp) c.660A>G c.2311A>G (p.Asn771Asp) c.*28+8392A>G (n.*28+8392A>G) c.2176A>G (p.Asn726Asp) n.1251T>C c.1510A>G (p.Asn504Asp) | ClinVar dbSNP |
7 | g.55181320A>T | CA367578656 | EGFR,EGFR-AS1 | c.2152A>T (p.Asn718Tyr) c.660A>T c.2311A>T (p.Asn771Tyr) c.*28+8392A>T (n.*28+8392A>T) c.2176A>T (p.Asn726Tyr) n.1251T>A c.1510A>T (p.Asn504Tyr) | |
7 | g.55181320delinsGGTT | CA645561589 | EGFR,EGFR-AS1 | c.2152delinsGGTT (p.Asn718delinsGlyTyr) c.660delinsGGTT c.2311delinsGGTT (p.Asn771delinsGlyTyr) c.*28+8392delinsGGTT (n.*28+8392delinsGGTT) c.2176delinsGGTT (p.Asn726delinsGlyTyr) n.1251delinsAACC c.1510delinsGGTT (p.Asn504delinsGlyTyr) | dbSNP COSMIC |
7 | g.55181320delinsGTCC | CA645561587 | EGFR,EGFR-AS1 | c.2152delinsGTCC (p.Asn718delinsValHis) c.660delinsGTCC c.2311delinsGTCC (p.Asn771delinsValHis) c.*28+8392delinsGTCC (n.*28+8392delinsGTCC) c.2176delinsGTCC (p.Asn726delinsValHis) n.1251delinsGGAC c.1510delinsGTCC (p.Asn504delinsValHis) | dbSNP COSMIC |
7 | g.55181320_55181321insGCGTCGAAA | CA645561593 | EGFR,EGFR-AS1 | c.2152_2153insGCGTCGAAA (p.Asp717_Asn718insSerValGlu) c.660_661insGCGTCGAAA c.2311_2312insGCGTCGAAA (p.Asp770_Asn771insSerValGlu) c.*28+8392_*28+8393insGCGTCGAAA (n.*28+8392_*28+8393insGCGTCGAAA) c.2176_2177insGCGTCGAAA (p.Asp725_Asn726insSerValGlu) n.1251_1252insTTCGACGCT c.1510_1511insGCGTCGAAA (p.Asp503_Asn504insSerValGlu) | dbSNP COSMIC |
7 | g.55181320_55181321delinsGGGTT | CA645561588 | EGFR,EGFR-AS1 | c.2152_2153delinsGGGTT (p.Asn718delinsGlyPhe) c.660_661delinsGGGTT c.2311_2312delinsGGGTT (p.Asn771delinsGlyPhe) c.*28+8392_*28+8393delinsGGGTT (n.*28+8392_*28+8393delinsGGGTT) c.2176_2177delinsGGGTT (p.Asn726delinsGlyPhe) n.1250_1251delinsAACCC c.1510_1511delinsGGGTT (p.Asn504delinsGlyPhe) | dbSNP COSMIC |
7 | g.55181320_55181324delinsAACCC | CA1708905213 | EGFR,EGFR-AS1 | c.2152_2156delinsAACCC (p.Asn718=) c.660_664delinsAACCC c.2311_2315delinsAACCC (p.Asn771=) c.*28+8392_*28+8396delinsAACCC (n.*28+8392_*28+8396delinsAACCC) c.2176_2180delinsAACCC (p.Asn726=) n.1247_1251delinsGGGTT c.1510_1514delinsAACCC (p.Asn504=) | |
7 | g.55181326_55181327insCGAACCCCC | CA181055 | EGFR,EGFR-AS1 | c.2158_2159insCGAACCCCC (p.Pro719_His720insProAsnPro) c.666_667insCGAACCCCC c.2317_2318insCGAACCCCC (p.Pro772_His773insProAsnPro) c.*28+8398_*28+8399insCGAACCCCC (n.*28+8398_*28+8399insCGAACCCCC) c.2182_2183insCGAACCCCC (p.Pro727_His728insProAsnPro) n.1251_1252insCGGGGGGTT c.1516_1517insCGAACCCCC (p.Pro505_His506insProAsnPro) | ClinVar dbSNP |
7 | g.55181320_55181321insCAC | CA180591 | EGFR,EGFR-AS1 | c.2152_2153insCAC (p.Asn718delinsThrHis) c.660_661insCAC c.2311_2312insCAC (p.Asn771delinsThrHis) c.*28+8392_*28+8393insCAC (n.*28+8392_*28+8393insCAC) c.2176_2177insCAC (p.Asn726delinsThrHis) n.1250_1251insGTG c.1510_1511insCAC (p.Asn504delinsThrHis) | ClinVar dbSNP COSMIC |
7 | g.55181320_55181321insGTC | CA645561596 | EGFR,EGFR-AS1 | c.2152_2153insGTC (p.Asn718delinsSerHis) c.660_661insGTC c.2311_2312insGTC (p.Asn771delinsSerHis) c.*28+8392_*28+8393insGTC (n.*28+8392_*28+8393insGTC) c.2176_2177insGTC (p.Asn726delinsSerHis) n.1250_1251insGAC c.1510_1511insGTC (p.Asn504delinsSerHis) | dbSNP COSMIC |
7 | g.55181320_55181321insGTT | CA176011 | EGFR,EGFR-AS1 | c.2152_2153insGTT (p.Asn718delinsSerTyr) c.660_661insGTT c.2311_2312insGTT (p.Asn771delinsSerTyr) c.*28+8392_*28+8393insGTT (n.*28+8392_*28+8393insGTT) c.2176_2177insGTT (p.Asn726delinsSerTyr) n.1250_1251insAAC c.1510_1511insGTT (p.Asn504delinsSerTyr) | ClinVar dbSNP |
7 | g.55181320_55181321insGTGGCC | CA645561597 | EGFR,EGFR-AS1 | c.2152_2153insGTGGCC (p.Asn718delinsSerGlyHis) c.660_661insGTGGCC c.2311_2312insGTGGCC (p.Asn771delinsSerGlyHis) c.*28+8392_*28+8393insGTGGCC (n.*28+8392_*28+8393insGTGGCC) c.2176_2177insGTGGCC (p.Asn726delinsSerGlyHis) n.1250_1251insGGCCAC c.1510_1511insGTGGCC (p.Asn504delinsSerGlyHis) | dbSNP COSMIC |
7 | g.55181320_55181321insCCCCCCACGTGT | CA2714569377 | EGFR,EGFR-AS1 | c.2152_2153insCCCCCCACGTGT (p.Asn718delinsThrProHisValTyr) c.660_661insCCCCCCACGTGT c.2311_2312insCCCCCCACGTGT (p.Asn771delinsThrProHisValTyr) c.*28+8392_*28+8393insCCCCCCACGTGT (n.*28+8392_*28+8393insCCCCCCACGTGT) c.2176_2177insCCCCCCACGTGT (p.Asn726delinsThrProHisValTyr) n.1250_1251insACACGTGGGGGG c.1510_1511insCCCCCCACGTGT (p.Asn504delinsThrProHisValTyr) | dbSNP |
7 | g.55181321A= | CA1708905239 | EGFR,EGFR-AS1 | c.2153A= (p.Asn718=) c.661A= c.2312A= (p.Asn771=) c.*28+8393A= (n.*28+8393A=) c.2177A= (p.Asn726=) n.1250T= c.1511A= (p.Asn504=) | |
7 | g.55181321A>C | CA367578660 | EGFR,EGFR-AS1 | c.2153A>C (p.Asn718Thr) c.661A>C c.2312A>C (p.Asn771Thr) c.*28+8393A>C (n.*28+8393A>C) c.2177A>C (p.Asn726Thr) n.1250T>G c.1511A>C (p.Asn504Thr) | dbSNP |
7 | g.55181321A>G | CA367578666 | EGFR,EGFR-AS1 | c.2153A>G (p.Asn718Ser) c.661A>G c.2312A>G (p.Asn771Ser) c.*28+8393A>G (n.*28+8393A>G) c.2177A>G (p.Asn726Ser) n.1250T>C c.1511A>G (p.Asn504Ser) | dbSNP gnomAD v4 |
7 | g.55181321A>T | CA367578664 | EGFR,EGFR-AS1 | c.2153A>T (p.Asn718Ile) c.661A>T c.2312A>T (p.Asn771Ile) c.*28+8393A>T (n.*28+8393A>T) c.2177A>T (p.Asn726Ile) n.1250T>A c.1511A>T (p.Asn504Ile) | |
7 | g.55181321_55181322insACA | CA2579986350 | EGFR,EGFR-AS1 | c.2153_2154insACA (p.Asn718delinsLysHis) c.661_662insACA c.2312_2313insACA (p.Asn771delinsLysHis) c.*28+8393_*28+8394insACA (n.*28+8393_*28+8394insACA) c.2177_2178insACA (p.Asn726delinsLysHis) n.1250_1251insGTT c.1511_1512insACA (p.Asn504delinsLysHis) | |
7 | g.55181323_55181324insACCACC | CA2714508310 | EGFR,EGFR-AS1 | c.2155_2156insACCACC (p.Asn718_Pro719insHisHis) c.663_664insACCACC c.2314_2315insACCACC (p.Asn771_Pro772insHisHis) c.*28+8395_*28+8396insACCACC (n.*28+8395_*28+8396insACCACC) c.2179_2180insACCACC (p.Asn726_Pro727insHisHis) n.1250_1251insGGTGGT c.1513_1514insACCACC (p.Asn504_Pro505insHisHis) | dbSNP |
7 | g.55181323_55181324insGGCACC | CA645561598 | EGFR,EGFR-AS1 | c.2155_2156insGGCACC (p.Asn718_Pro719insArgHis) c.663_664insGGCACC c.2314_2315insGGCACC (p.Asn771_Pro772insArgHis) c.*28+8395_*28+8396insGGCACC (n.*28+8395_*28+8396insGGCACC) c.2179_2180insGGCACC (p.Asn726_Pro727insArgHis) n.1250_1251insGCCGGT c.1513_1514insGGCACC (p.Asn504_Pro505insArgHis) | dbSNP COSMIC |
7 | g.55181321_55181323dup | CA135857 | EGFR,EGFR-AS1 | c.2153_2155dup (p.Asn718_Pro719insHis) c.661_663dup c.2312_2314dup (p.Asn771_Pro772insHis) c.*28+8393_*28+8395dup (n.*28+8393_*28+8395dup) c.2177_2179dup (p.Asn726_Pro727insHis) n.1248_1250dup c.1511_1513dup (p.Asn504_Pro505insHis) | ClinVar dbSNP COSMIC |
7 | g.55181321_55181324delinsGCGTGGACAACCG | CA158928351 | EGFR,EGFR-AS1 | c.2153_2156delinsGCGTGGACAACCG (p.Asn718_Pro719delinsSerValAspAsnArg) c.661_664delinsGCGTGGACAACCG c.2312_2315delinsGCGTGGACAACCG (p.Asn771_Pro772delinsSerValAspAsnArg) c.*28+8393_*28+8396delinsGCGTGGACAACCG (n.*28+8393_*28+8396delinsGCGTGGACAACCG) c.2177_2180delinsGCGTGGACAACCG (p.Asn726_Pro727delinsSerValAspAsnArg) n.1247_1250delinsCGGTTGTCCACGC c.1511_1514delinsGCGTGGACAACCG (p.Asn504_Pro505delinsSerValAspAsnArg) | dbSNP COSMIC |
7 | g.55181324_55181325insGACACACCC | CA645561594 | EGFR,EGFR-AS1 | c.2156_2157insGACACACCC (p.Pro719_His720insThrHisPro) c.664_665insGACACACCC c.2315_2316insGACACACCC (p.Pro772_His773insThrHisPro) c.*28+8396_*28+8397insGACACACCC (n.*28+8396_*28+8397insGACACACCC) c.2180_2181insGACACACCC (p.Pro727_His728insThrHisPro) n.1250_1251insGTGTCGGGT c.1514_1515insGACACACCC (p.Pro505_His506insThrHisPro) | dbSNP COSMIC |
7 | g.55181326_55181327insCCCACCCCC | CA891842015 | EGFR,EGFR-AS1 | c.2158_2159insCCCACCCCC (p.Pro719_His720insProHisPro) c.666_667insCCCACCCCC c.2317_2318insCCCACCCCC (p.Pro772_His773insProHisPro) c.*28+8398_*28+8399insCCCACCCCC (n.*28+8398_*28+8399insCCCACCCCC) c.2182_2183insCCCACCCCC (p.Pro727_His728insProHisPro) n.1250_1251insGGGGGGGGT c.1516_1517insCCCACCCCC (p.Pro505_His506insProHisPro) | |
7 | g.55181323_55181328dup | CA645561595 | EGFR,EGFR-AS1 | c.2155_2160dup (p.His720_Val721insProHis) c.663_668dup c.2314_2319dup (p.His773_Val774insProHis) c.*28+8395_*28+8400dup (n.*28+8395_*28+8400dup) c.2179_2184dup (p.His728_Val729insProHis) n.1245_1250dup c.1513_1518dup (p.His506_Val507insProHis) | dbSNP COSMIC COSMIC |
7 | g.55181321_55181322insACT | CA645561599 | EGFR,EGFR-AS1 | c.2153_2154insACT (p.Asn718delinsLysLeu) c.661_662insACT c.2312_2313insACT (p.Asn771delinsLysLeu) c.*28+8393_*28+8394insACT (n.*28+8393_*28+8394insACT) c.2177_2178insACT (p.Asn726delinsLysLeu) n.1249_1250insAGT c.1511_1512insACT (p.Asn504delinsLysLeu) | dbSNP COSMIC |
7 | g.55181321_55181322insTGT | CA176017 | EGFR,EGFR-AS1 | c.2153_2154insTGT (p.Asn718_Pro719insVal) c.661_662insTGT c.2312_2313insTGT (p.Asn771_Pro772insVal) c.*28+8393_*28+8394insTGT (n.*28+8393_*28+8394insTGT) c.2177_2178insTGT (p.Asn726_Pro727insVal) n.1249_1250insACA c.1511_1512insTGT (p.Asn504_Pro505insVal) | ClinVar dbSNP |
7 | g.55181321_55181322insGCCCCACGTGTG | CA2714511591 | EGFR,EGFR-AS1 | c.2153_2154insGCCCCACGTGTG (p.Asn718delinsLysProHisValCys) c.661_662insGCCCCACGTGTG c.2312_2313insGCCCCACGTGTG (p.Asn771delinsLysProHisValCys) c.*28+8393_*28+8394insGCCCCACGTGTG (n.*28+8393_*28+8394insGCCCCACGTGTG) c.2177_2178insGCCCCACGTGTG (p.Asn726delinsLysProHisValCys) n.1249_1250insCACACGTGGGGC c.1511_1512insGCCCCACGTGTG (p.Asn504delinsLysProHisValCys) | dbSNP |
7 | g.55181321_55181322insTCCCCACGTGTG | CA2714511592 | EGFR,EGFR-AS1 | c.2153_2154insTCCCCACGTGTG (p.Asn718_Pro719insProHisValCys) c.661_662insTCCCCACGTGTG c.2312_2313insTCCCCACGTGTG (p.Asn771_Pro772insProHisValCys) c.*28+8393_*28+8394insTCCCCACGTGTG (n.*28+8393_*28+8394insTCCCCACGTGTG) c.2177_2178insTCCCCACGTGTG (p.Asn726_Pro727insProHisValCys) n.1249_1250insCACACGTGGGGA c.1511_1512insTCCCCACGTGTG (p.Asn504_Pro505insProHisValCys) | dbSNP |
7 | g.55181321_55181322insGATACAACCCCCACGTGTG | CA2714511593 | EGFR,EGFR-AS1 | c.2153_2154insGATACAACCCCCACGTGTG (p.Asn718LysfsTer?) c.661_662insGATACAACCCCCACGTGTG c.2312_2313insGATACAACCCCCACGTGTG (p.Asn771LysfsTer?) c.*28+8393_*28+8394insGATACAACCCCCACGTGTG (n.*28+8393_*28+8394insGATACAACCCCCACGTGTG) c.2177_2178insGATACAACCCCCACGTGTG (p.Asn726LysfsTer?) n.1249_1250insCACACGTGGGGGTTGTATC c.1511_1512insGATACAACCCCCACGTGTG (p.Asn504LysfsTer?) | dbSNP |
7 | g.55181322C>A | CA367578670 | EGFR,EGFR-AS1 | c.2154C>A (p.Asn718Lys) c.662C>A c.2313C>A (p.Asn771Lys) c.*28+8394C>A (n.*28+8394C>A) c.2178C>A (p.Asn726Lys) n.1249G>T c.1512C>A (p.Asn504Lys) | ClinVar |
7 | g.55181322C>G | CA367578672 | EGFR,EGFR-AS1 | c.2154C>G (p.Asn718Lys) c.662C>G c.2313C>G (p.Asn771Lys) c.*28+8394C>G (n.*28+8394C>G) c.2178C>G (p.Asn726Lys) n.1249G>C c.1512C>G (p.Asn504Lys) | |
7 | g.55181322C>T | CA455165084 | EGFR,EGFR-AS1 | c.2154C>T (p.Asn718=) c.662C>T c.2313C>T (p.Asn771=) c.*28+8394C>T (n.*28+8394C>T) c.2178C>T (p.Asn726=) n.1249G>A c.1512C>T (p.Asn504=) | dbSNP gnomAD v4 |
7 | g.55181322_55181323insACCCACGTGTGC | CA2714933600 | EGFR,EGFR-AS1 | c.2154_2155insACCCACGTGTGC (p.Asn718_Pro719insThrHisValCys) c.662_663insACCCACGTGTGC c.2313_2314insACCCACGTGTGC (p.Asn771_Pro772insThrHisValCys) c.*28+8394_*28+8395insACCCACGTGTGC (n.*28+8394_*28+8395insACCCACGTGTGC) c.2178_2179insACCCACGTGTGC (p.Asn726_Pro727insThrHisValCys) n.1249_1250insCACACGTGGGTG c.1512_1513insACCCACGTGTGC (p.Asn504_Pro505insThrHisValCys) | dbSNP |
7 | g.55181322_55181323insGCCCACGTGTGC | CA2714933155 | EGFR,EGFR-AS1 | c.2154_2155insGCCCACGTGTGC (p.Asn718_Pro719insAlaHisValCys) c.662_663insGCCCACGTGTGC c.2313_2314insGCCCACGTGTGC (p.Asn771_Pro772insAlaHisValCys) c.*28+8394_*28+8395insGCCCACGTGTGC (n.*28+8394_*28+8395insGCCCACGTGTGC) c.2178_2179insGCCCACGTGTGC (p.Asn726_Pro727insAlaHisValCys) n.1249_1250insCACACGTGGGCG c.1512_1513insGCCCACGTGTGC (p.Asn504_Pro505insAlaHisValCys) | dbSNP |
7 | g.55181322_55181323insTCCCACGTGTGC | CA2714933023 | EGFR,EGFR-AS1 | c.2154_2155insTCCCACGTGTGC (p.Asn718_Pro719insSerHisValCys) c.662_663insTCCCACGTGTGC c.2313_2314insTCCCACGTGTGC (p.Asn771_Pro772insSerHisValCys) c.*28+8394_*28+8395insTCCCACGTGTGC (n.*28+8394_*28+8395insTCCCACGTGTGC) c.2178_2179insTCCCACGTGTGC (p.Asn726_Pro727insSerHisValCys) n.1249_1250insCACACGTGGGAG c.1512_1513insTCCCACGTGTGC (p.Asn504_Pro505insSerHisValCys) | dbSNP |
7 | g.55181323_55181324insACCACGTGTGCC | CA2714933355 | EGFR,EGFR-AS1 | c.2155_2156insACCACGTGTGCC (p.Asn718_Pro719insHisHisValCys) c.663_664insACCACGTGTGCC c.2314_2315insACCACGTGTGCC (p.Asn771_Pro772insHisHisValCys) c.*28+8395_*28+8396insACCACGTGTGCC (n.*28+8395_*28+8396insACCACGTGTGCC) c.2179_2180insACCACGTGTGCC (p.Asn726_Pro727insHisHisValCys) n.1249_1250insCACACGTGGTGG c.1513_1514insACCACGTGTGCC (p.Asn504_Pro505insHisHisValCys) | dbSNP |
7 | g.55181323_55181324insGCCACGTGTGCC | CA2714933104 | EGFR,EGFR-AS1 | c.2155_2156insGCCACGTGTGCC (p.Asn718_Pro719insArgHisValCys) c.663_664insGCCACGTGTGCC c.2314_2315insGCCACGTGTGCC (p.Asn771_Pro772insArgHisValCys) c.*28+8395_*28+8396insGCCACGTGTGCC (n.*28+8395_*28+8396insGCCACGTGTGCC) c.2179_2180insGCCACGTGTGCC (p.Asn726_Pro727insArgHisValCys) n.1249_1250insCACACGTGGCGG c.1513_1514insGCCACGTGTGCC (p.Asn504_Pro505insArgHisValCys) | dbSNP |
7 | g.55181323_55181324insGCCAGGTGTGCC | CA2714933588 | EGFR,EGFR-AS1 | c.2155_2156insGCCAGGTGTGCC (p.Asn718_Pro719insArgGlnValCys) c.663_664insGCCAGGTGTGCC c.2314_2315insGCCAGGTGTGCC (p.Asn771_Pro772insArgGlnValCys) c.*28+8395_*28+8396insGCCAGGTGTGCC (n.*28+8395_*28+8396insGCCAGGTGTGCC) c.2179_2180insGCCAGGTGTGCC (p.Asn726_Pro727insArgGlnValCys) n.1249_1250insCACACCTGGCGG c.1513_1514insGCCAGGTGTGCC (p.Asn504_Pro505insArgGlnValCys) | dbSNP |
7 | g.55181323_55181324insTCCACGTGTGCC | CA2714933430 | EGFR,EGFR-AS1 | c.2155_2156insTCCACGTGTGCC (p.Asn718_Pro719insLeuHisValCys) c.663_664insTCCACGTGTGCC c.2314_2315insTCCACGTGTGCC (p.Asn771_Pro772insLeuHisValCys) c.*28+8395_*28+8396insTCCACGTGTGCC (n.*28+8395_*28+8396insTCCACGTGTGCC) c.2179_2180insTCCACGTGTGCC (p.Asn726_Pro727insLeuHisValCys) n.1249_1250insCACACGTGGAGG c.1513_1514insTCCACGTGTGCC (p.Asn504_Pro505insLeuHisValCys) | dbSNP |
7 | g.55181324_55181325insACACGTCTGCCC | CA2714933500 | EGFR,EGFR-AS1 | c.2156_2157insACACGTCTGCCC (p.Pro719_His720insHisValCysPro) c.664_665insACACGTCTGCCC c.2315_2316insACACGTCTGCCC (p.Pro772_His773insHisValCysPro) c.*28+8396_*28+8397insACACGTCTGCCC (n.*28+8396_*28+8397insACACGTCTGCCC) c.2180_2181insACACGTCTGCCC (p.Pro727_His728insHisValCysPro) n.1249_1250insCAGACGTGTGGG c.1514_1515insACACGTCTGCCC (p.Pro505_His506insHisValCysPro) | dbSNP |
7 | g.55181324_55181325insACACGTGTGCCC | CA2714933417 | EGFR,EGFR-AS1 | c.2156_2157insACACGTGTGCCC (p.Pro719_His720insHisValCysPro) c.664_665insACACGTGTGCCC c.2315_2316insACACGTGTGCCC (p.Pro772_His773insHisValCysPro) c.*28+8396_*28+8397insACACGTGTGCCC (n.*28+8396_*28+8397insACACGTGTGCCC) c.2180_2181insACACGTGTGCCC (p.Pro727_His728insHisValCysPro) n.1249_1250insCACACGTGTGGG c.1514_1515insACACGTGTGCCC (p.Pro505_His506insHisValCysPro) | dbSNP |
7 | g.55181324_55181325insGCACGTGTGCCC | CA2714933147 | EGFR,EGFR-AS1 | c.2156_2157insGCACGTGTGCCC (p.Pro719_His720insHisValCysPro) c.664_665insGCACGTGTGCCC c.2315_2316insGCACGTGTGCCC (p.Pro772_His773insHisValCysPro) c.*28+8396_*28+8397insGCACGTGTGCCC (n.*28+8396_*28+8397insGCACGTGTGCCC) c.2180_2181insGCACGTGTGCCC (p.Pro727_His728insHisValCysPro) n.1249_1250insCACACGTGCGGG c.1514_1515insGCACGTGTGCCC (p.Pro505_His506insHisValCysPro) | dbSNP |
7 | g.55181324_55181325insGCCCGTGTGCCC | CA2714932987 | EGFR,EGFR-AS1 | c.2156_2157insGCCCGTGTGCCC (p.Pro719_His720insProValCysPro) c.664_665insGCCCGTGTGCCC c.2315_2316insGCCCGTGTGCCC (p.Pro772_His773insProValCysPro) c.*28+8396_*28+8397insGCCCGTGTGCCC (n.*28+8396_*28+8397insGCCCGTGTGCCC) c.2180_2181insGCCCGTGTGCCC (p.Pro727_His728insProValCysPro) n.1249_1250insCACACGGGCGGG c.1514_1515insGCCCGTGTGCCC (p.Pro505_His506insProValCysPro) | dbSNP |
7 | g.55181324_55181325insTCACGTGTGCCC | CA2714933150 | EGFR,EGFR-AS1 | c.2156_2157insTCACGTGTGCCC (p.Pro719_His720insHisValCysPro) c.664_665insTCACGTGTGCCC c.2315_2316insTCACGTGTGCCC (p.Pro772_His773insHisValCysPro) c.*28+8396_*28+8397insTCACGTGTGCCC (n.*28+8396_*28+8397insTCACGTGTGCCC) c.2180_2181insTCACGTGTGCCC (p.Pro727_His728insHisValCysPro) n.1249_1250insCACACGTGAGGG c.1514_1515insTCACGTGTGCCC (p.Pro505_His506insHisValCysPro) | dbSNP |
7 | g.55181325_55181326insACGTGTGCCCC | CA2714933102 | EGFR,EGFR-AS1 | c.2157_2158insACGTGTGCCCC (p.His720ThrfsTer?) c.665_666insACGTGTGCCCC c.2316_2317insACGTGTGCCCC (p.His773ThrfsTer?) c.*28+8397_*28+8398insACGTGTGCCCC (n.*28+8397_*28+8398insACGTGTGCCCC) c.2181_2182insACGTGTGCCCC (p.His728ThrfsTer?) n.1249_1250insCACACGTGGGG c.1515_1516insACGTGTGCCCC (p.His506ThrfsTer?) | dbSNP |
7 | g.55181326_55181327insCCGTGTGCCCCC | CA2714933099 | EGFR,EGFR-AS1 | c.2158_2159insCCGTGTGCCCCC (p.Pro719_His720insProValCysPro) c.666_667insCCGTGTGCCCCC c.2317_2318insCCGTGTGCCCCC (p.Pro772_His773insProValCysPro) c.*28+8398_*28+8399insCCGTGTGCCCCC (n.*28+8398_*28+8399insCCGTGTGCCCCC) c.2182_2183insCCGTGTGCCCCC (p.Pro727_His728insProValCysPro) n.1249_1250insCACACGGGGGGG c.1516_1517insCCGTGTGCCCCC (p.Pro505_His506insProValCysPro) | dbSNP |
7 | g.55181326_55181327insGCGTGTGCCCCC | CA2714933605 | EGFR,EGFR-AS1 | c.2158_2159insGCGTGTGCCCCC (p.Pro719_His720insArgValCysPro) c.666_667insGCGTGTGCCCCC c.2317_2318insGCGTGTGCCCCC (p.Pro772_His773insArgValCysPro) c.*28+8398_*28+8399insGCGTGTGCCCCC (n.*28+8398_*28+8399insGCGTGTGCCCCC) c.2182_2183insGCGTGTGCCCCC (p.Pro727_His728insArgValCysPro) n.1249_1250insCACACGCGGGGG c.1516_1517insGCGTGTGCCCCC (p.Pro505_His506insArgValCysPro) | dbSNP |
7 | g.55181326_55181327insTCGTGTGCCCCC | CA2714933154 | EGFR,EGFR-AS1 | c.2158_2159insTCGTGTGCCCCC (p.Pro719_His720insLeuValCysPro) c.666_667insTCGTGTGCCCCC c.2317_2318insTCGTGTGCCCCC (p.Pro772_His773insLeuValCysPro) c.*28+8398_*28+8399insTCGTGTGCCCCC (n.*28+8398_*28+8399insTCGTGTGCCCCC) c.2182_2183insTCGTGTGCCCCC (p.Pro727_His728insLeuValCysPro) n.1249_1250insCACACGAGGGGG c.1516_1517insTCGTGTGCCCCC (p.Pro505_His506insLeuValCysPro) | dbSNP |
7 | g.55181326_55181327insCACGTGTGCCCCC | CA2714933618 | EGFR,EGFR-AS1 | c.2158_2159insCACGTGTGCCCCC (p.His720ProfsTer?) c.666_667insCACGTGTGCCCCC c.2317_2318insCACGTGTGCCCCC (p.His773ProfsTer?) c.*28+8398_*28+8399insCACGTGTGCCCCC (n.*28+8398_*28+8399insCACGTGTGCCCCC) c.2182_2183insCACGTGTGCCCCC (p.His728ProfsTer?) n.1249_1250insCACACGTGGGGGG c.1516_1517insCACGTGTGCCCCC (p.His506ProfsTer?) | dbSNP |
7 | g.55181326del | CA891842016 | EGFR,EGFR-AS1 | c.2158del (p.His720ThrfsTer?) c.666del c.2317del (p.His773ThrfsTer?) c.*28+8398del (n.*28+8398del) c.2182del (p.His728ThrfsTer?) n.1249del c.1516del (p.His506ThrfsTer?) | dbSNP |
7 | g.55181327_55181328insAGTGTGCCCCCA | CA2714933194 | EGFR,EGFR-AS1 | c.2159_2160insAGTGTGCCCCCA (p.Pro719_His720insGlnValCysPro) c.667_668insAGTGTGCCCCCA c.2318_2319insAGTGTGCCCCCA (p.Pro772_His773insGlnValCysPro) c.*28+8399_*28+8400insAGTGTGCCCCCA (n.*28+8399_*28+8400insAGTGTGCCCCCA) c.2183_2184insAGTGTGCCCCCA (p.Pro727_His728insGlnValCysPro) n.1249_1250insCACACTTGGGGG c.1517_1518insAGTGTGCCCCCA (p.Pro505_His506insGlnValCysPro) | dbSNP |
7 | g.55181327_55181328insTGTGTGCCCCCA | CA2714933270 | EGFR,EGFR-AS1 | c.2159_2160insTGTGTGCCCCCA (p.His720_Val721insValCysProHis) c.667_668insTGTGTGCCCCCA c.2318_2319insTGTGTGCCCCCA (p.His773_Val774insValCysProHis) c.*28+8399_*28+8400insTGTGTGCCCCCA (n.*28+8399_*28+8400insTGTGTGCCCCCA) c.2183_2184insTGTGTGCCCCCA (p.His728_Val729insValCysProHis) n.1249_1250insCACACATGGGGG c.1517_1518insTGTGTGCCCCCA (p.His506_Val507insValCysProHis) | dbSNP |
7 | g.55181328_55181329insATGTGCCCCCAC | CA2714933315 | EGFR,EGFR-AS1 | c.2160_2161insATGTGCCCCCAC (p.His720_Val721insMetCysProHis) c.668_669insATGTGCCCCCAC c.2319_2320insATGTGCCCCCAC (p.His773_Val774insMetCysProHis) c.*28+8400_*28+8401insATGTGCCCCCAC (n.*28+8400_*28+8401insATGTGCCCCCAC) c.2184_2185insATGTGCCCCCAC (p.His728_Val729insMetCysProHis) n.1249_1250insCACATGTGGGGG c.1518_1519insATGTGCCCCCAC (p.His506_Val507insMetCysProHis) | dbSNP |
7 | g.55181328_55181329insCTGTGCCCCCAC | CA2714933353 | EGFR,EGFR-AS1 | c.2160_2161insCTGTGCCCCCAC (p.His720_Val721insLeuCysProHis) c.668_669insCTGTGCCCCCAC c.2319_2320insCTGTGCCCCCAC (p.His773_Val774insLeuCysProHis) c.*28+8400_*28+8401insCTGTGCCCCCAC (n.*28+8400_*28+8401insCTGTGCCCCCAC) c.2184_2185insCTGTGCCCCCAC (p.His728_Val729insLeuCysProHis) n.1249_1250insCACAGGTGGGGG c.1518_1519insCTGTGCCCCCAC (p.His506_Val507insLeuCysProHis) | dbSNP |
7 | g.55181329_55181330insAGTGCCCCCACG | CA2714933193 | EGFR,EGFR-AS1 | c.2161_2162insAGTGCCCCCACG (p.His720_Val721insGluCysProHis) c.669_670insAGTGCCCCCACG c.2320_2321insAGTGCCCCCACG (p.His773_Val774insGluCysProHis) c.*28+8401_*28+8402insAGTGCCCCCACG (n.*28+8401_*28+8402insAGTGCCCCCACG) c.2185_2186insAGTGCCCCCACG (p.His728_Val729insGluCysProHis) n.1249_1250insCACTCGTGGGGG c.1519_1520insAGTGCCCCCACG (p.His506_Val507insGluCysProHis) | dbSNP |
7 | g.55181329_55181330insCGTGCCCCCACG | CA2714933318 | EGFR,EGFR-AS1 | c.2161_2162insCGTGCCCCCACG (p.His720_Val721insAlaCysProHis) c.669_670insCGTGCCCCCACG c.2320_2321insCGTGCCCCCACG (p.His773_Val774insAlaCysProHis) c.*28+8401_*28+8402insCGTGCCCCCACG (n.*28+8401_*28+8402insCGTGCCCCCACG) c.2185_2186insCGTGCCCCCACG (p.His728_Val729insAlaCysProHis) n.1249_1250insCACGCGTGGGGG c.1519_1520insCGTGCCCCCACG (p.His506_Val507insAlaCysProHis) | dbSNP |
7 | g.55181329_55181330insGGGGCCCCCACG | CA2714933305 | EGFR,EGFR-AS1 | c.2161_2162insGGGGCCCCCACG (p.His720_Val721insGlyGlyProHis) c.669_670insGGGGCCCCCACG c.2320_2321insGGGGCCCCCACG (p.His773_Val774insGlyGlyProHis) c.*28+8401_*28+8402insGGGGCCCCCACG (n.*28+8401_*28+8402insGGGGCCCCCACG) c.2185_2186insGGGGCCCCCACG (p.His728_Val729insGlyGlyProHis) n.1249_1250insCCCCCGTGGGGG c.1519_1520insGGGGCCCCCACG (p.His506_Val507insGlyGlyProHis) | dbSNP |
7 | g.55181329_55181330insGGTGCCCCCACG | CA2714933226 | EGFR,EGFR-AS1 | c.2161_2162insGGTGCCCCCACG (p.His720_Val721insGlyCysProHis) c.669_670insGGTGCCCCCACG c.2320_2321insGGTGCCCCCACG (p.His773_Val774insGlyCysProHis) c.*28+8401_*28+8402insGGTGCCCCCACG (n.*28+8401_*28+8402insGGTGCCCCCACG) c.2185_2186insGGTGCCCCCACG (p.His728_Val729insGlyCysProHis) n.1249_1250insCACCCGTGGGGG c.1519_1520insGGTGCCCCCACG (p.His506_Val507insGlyCysProHis) | dbSNP |
7 | g.55181330_55181331insCTGCCCCCACGT | CA2714508311 | EGFR,EGFR-AS1 | c.2162_2163insCTGCCCCCACGT (p.Val721_Cys722insCysProHisVal) c.670_671insCTGCCCCCACGT c.2321_2322insCTGCCCCCACGT (p.Val774_Cys775insCysProHisVal) c.*28+8402_*28+8403insCTGCCCCCACGT (n.*28+8402_*28+8403insCTGCCCCCACGT) c.2186_2187insCTGCCCCCACGT (p.Val729_Cys730insCysProHisVal) n.1249_1250insCAGACGTGGGGG c.1520_1521insCTGCCCCCACGT (p.Val507_Cys508insCysProHisVal) | dbSNP |
7 | g.55181322_55181330dup | CA135860 | EGFR,EGFR-AS1 | c.2154_2162dup (p.Val721_Cys722insProHisVal) c.662_670dup c.2313_2321dup (p.Val774_Cys775insProHisVal) c.*28+8394_*28+8402dup (n.*28+8394_*28+8402dup) c.2178_2186dup (p.Val729_Cys730insProHisVal) n.1241_1249dup c.1512_1520dup (p.Val507_Cys508insProHisVal) | ClinVar dbSNP |
7 | g.55181331_55181332insAGCCCCCACGTG | CA2714933196 | EGFR,EGFR-AS1 | c.2163_2164insAGCCCCCACGTG (p.Val721_Cys722insSerProHisVal) c.671_672insAGCCCCCACGTG c.2322_2323insAGCCCCCACGTG (p.Val774_Cys775insSerProHisVal) c.*28+8403_*28+8404insAGCCCCCACGTG (n.*28+8403_*28+8404insAGCCCCCACGTG) c.2187_2188insAGCCCCCACGTG (p.Val729_Cys730insSerProHisVal) n.1249_1250insCTCACGTGGGGG c.1521_1522insAGCCCCCACGTG (p.Val507_Cys508insSerProHisVal) | dbSNP |
7 | g.55181331_55181332insGGCCCCCACGTG | CA2714933190 | EGFR,EGFR-AS1 | c.2163_2164insGGCCCCCACGTG (p.Val721_Cys722insGlyProHisVal) c.671_672insGGCCCCCACGTG c.2322_2323insGGCCCCCACGTG (p.Val774_Cys775insGlyProHisVal) c.*28+8403_*28+8404insGGCCCCCACGTG (n.*28+8403_*28+8404insGGCCCCCACGTG) c.2187_2188insGGCCCCCACGTG (p.Val729_Cys730insGlyProHisVal) n.1249_1250insCCCACGTGGGGG c.1521_1522insGGCCCCCACGTG (p.Val507_Cys508insGlyProHisVal) | dbSNP |
7 | g.55181324_55181335dup | CA2714933161 | EGFR,EGFR-AS1 | c.2156_2167dup (p.Cys722_Arg723insProHisValCys) c.664_675dup c.2315_2326dup (p.Cys775_Arg776insProHisValCys) c.*28+8396_*28+8407dup (n.*28+8396_*28+8407dup) c.2180_2191dup (p.Cys730_Arg731insProHisValCys) n.1238_1249dup c.1514_1525dup (p.Cys508_Arg509insProHisValCys) | dbSNP |
7 | g.55181322_55181323insACA | CA891842017 | EGFR,EGFR-AS1 | c.2154_2155insACA (p.Asn718_Pro719insThr) c.662_663insACA c.2313_2314insACA (p.Asn771_Pro772insThr) c.*28+8394_*28+8395insACA (n.*28+8394_*28+8395insACA) c.2178_2179insACA (p.Asn726_Pro727insThr) n.1248_1249insTGT c.1512_1513insACA (p.Asn504_Pro505insThr) | |
7 | g.55181322_55181323insTTA | CA2573102929 | EGFR,EGFR-AS1 | c.2154_2155insTTA (p.Asn718_Pro719insLeu) c.662_663insTTA c.2313_2314insTTA (p.Asn771_Pro772insLeu) c.*28+8394_*28+8395insTTA (n.*28+8394_*28+8395insTTA) c.2178_2179insTTA (p.Asn726_Pro727insLeu) n.1248_1249insTAA c.1512_1513insTTA (p.Asn504_Pro505insLeu) | |
7 | g.55181323C>A | CA367578678 | EGFR,EGFR-AS1 | c.2155C>A (p.Pro719Thr) c.663C>A c.2314C>A (p.Pro772Thr) c.*28+8395C>A (n.*28+8395C>A) c.2179C>A (p.Pro727Thr) n.1248G>T c.1513C>A (p.Pro505Thr) | |
7 | g.55181323C= | CA1708905273 | EGFR,EGFR-AS1 | c.2155C= (p.Pro719=) c.663C= c.2314C= (p.Pro772=) c.*28+8395C= (n.*28+8395C=) c.2179C= (p.Pro727=) n.1248G= c.1513C= (p.Pro505=) | |
7 | g.55181323C>G | CA4266053 | EGFR,EGFR-AS1 | c.2155C>G (p.Pro719Ala) c.663C>G c.2314C>G (p.Pro772Ala) c.*28+8395C>G (n.*28+8395C>G) c.2179C>G (p.Pro727Ala) n.1248G>C c.1513C>G (p.Pro505Ala) | dbSNP ExAC gnomAD v2 gnomAD v4 |
7 | g.55181323C>T | CA367578680 | EGFR,EGFR-AS1 | c.2155C>T (p.Pro719Ser) c.663C>T c.2314C>T (p.Pro772Ser) c.*28+8395C>T (n.*28+8395C>T) c.2179C>T (p.Pro727Ser) n.1248G>A c.1513C>T (p.Pro505Ser) | |
7 | g.55181325_55181326insTATAATCCC | CA2573051294 | EGFR,EGFR-AS1 | c.2157_2158insTATAATCCC (p.Pro719_His720insTyrAsnPro) c.665_666insTATAATCCC c.2316_2317insTATAATCCC (p.Pro772_His773insTyrAsnPro) c.*28+8397_*28+8398insTATAATCCC (n.*28+8397_*28+8398insTATAATCCC) c.2181_2182insTATAATCCC (p.Pro727_His728insTyrAsnPro) n.1248_1249insATTATAGGG c.1515_1516insTATAATCCC (p.Pro505_His506insTyrAsnPro) | |
7 | g.55181326_55181327insGTTGTCCCC | CA891842018 | EGFR,EGFR-AS1 | c.2158_2159insGTTGTCCCC (p.Pro719_His720insArgCysPro) c.666_667insGTTGTCCCC c.2317_2318insGTTGTCCCC (p.Pro772_His773insArgCysPro) c.*28+8398_*28+8399insGTTGTCCCC (n.*28+8398_*28+8399insGTTGTCCCC) c.2182_2183insGTTGTCCCC (p.Pro727_His728insArgCysPro) n.1248_1249insACAACGGGG c.1516_1517insGTTGTCCCC (p.Pro505_His506insArgCysPro) | |
7 | g.55181323_55181331dup | CA2573051293 | EGFR,EGFR-AS1 | c.2155_2163dup (p.Val721_Cys722insProHisVal) c.663_671dup c.2314_2322dup (p.Val774_Cys775insProHisVal) c.*28+8395_*28+8403dup (n.*28+8395_*28+8403dup) c.2179_2187dup (p.Val729_Cys730insProHisVal) n.1240_1248dup c.1513_1521dup (p.Val507_Cys508insProHisVal) | |
7 | g.55181333_55181334insTCCCCACGTGTG | CA2714933663 | EGFR,EGFR-AS1 | c.2165_2166insTCCCCACGTGTG (p.Cys722_Arg723insProHisValCys) c.673_674insTCCCCACGTGTG c.2324_2325insTCCCCACGTGTG (p.Cys775_Arg776insProHisValCys) c.*28+8405_*28+8406insTCCCCACGTGTG (n.*28+8405_*28+8406insTCCCCACGTGTG) c.2189_2190insTCCCCACGTGTG (p.Cys730_Arg731insProHisValCys) n.1248_1249insACACACGTGGGG c.1523_1524insTCCCCACGTGTG (p.Cys508_Arg509insProHisValCys) | dbSNP |
7 | g.55181324C>A | CA367578690 | EGFR,EGFR-AS1 | c.2156C>A (p.Pro719His) c.664C>A c.2315C>A (p.Pro772His) c.*28+8396C>A (n.*28+8396C>A) c.2180C>A (p.Pro727His) n.1247G>T c.1514C>A (p.Pro505His) | |
7 | g.55181324C= | CA1708905277 | EGFR,EGFR-AS1 | c.2156C= (p.Pro719=) c.664C= c.2315C= (p.Pro772=) c.*28+8396C= (n.*28+8396C=) c.2180C= (p.Pro727=) n.1247G= c.1514C= (p.Pro505=) | |
7 | g.55181324C>G | CA367578687 | EGFR,EGFR-AS1 | c.2156C>G (p.Pro719Arg) c.664C>G c.2315C>G (p.Pro772Arg) c.*28+8396C>G (n.*28+8396C>G) c.2180C>G (p.Pro727Arg) n.1247G>C c.1514C>G (p.Pro505Arg) | COSMIC |
7 | g.55181324C>T | CA367578683 | EGFR,EGFR-AS1 | c.2156C>T (p.Pro719Leu) c.664C>T c.2315C>T (p.Pro772Leu) c.*28+8396C>T (n.*28+8396C>T) c.2180C>T (p.Pro727Leu) n.1247G>A c.1514C>T (p.Pro505Leu) | COSMIC |
7 | g.55181324_55181329dup | CA135863 | EGFR,EGFR-AS1 | c.2156_2161dup (p.His720_Val721insAlaHis) c.664_669dup c.2315_2320dup (p.His773_Val774insAlaHis) c.*28+8396_*28+8401dup (n.*28+8396_*28+8401dup) c.2180_2185dup (p.His728_Val729insAlaHis) n.1242_1247dup c.1514_1519dup (p.His506_Val507insAlaHis) | ClinVar dbSNP COSMIC |
7 | g.55181325C>A | CA455165086 | EGFR,EGFR-AS1 | c.2157C>A (p.Pro719=) c.665C>A c.2316C>A (p.Pro772=) c.*28+8397C>A (n.*28+8397C>A) c.2181C>A (p.Pro727=) n.1246G>T c.1515C>A (p.Pro505=) | |
7 | g.55181325C= | CA1708905291 | EGFR,EGFR-AS1 | c.2157C= (p.Pro719=) c.665C= c.2316C= (p.Pro772=) c.*28+8397C= (n.*28+8397C=) c.2181C= (p.Pro727=) n.1246G= c.1515C= (p.Pro505=) | |
7 | g.55181325C>G | CA158928400 | EGFR,EGFR-AS1 | c.2157C>G (p.Pro719=) c.665C>G c.2316C>G (p.Pro772=) c.*28+8397C>G (n.*28+8397C>G) c.2181C>G (p.Pro727=) n.1246G>C c.1515C>G (p.Pro505=) | dbSNP |
7 | g.55181325C>T | CA455165087 | EGFR,EGFR-AS1 | c.2157C>T (p.Pro719=) c.665C>T c.2316C>T (p.Pro772=) c.*28+8397C>T (n.*28+8397C>T) c.2181C>T (p.Pro727=) n.1246G>A c.1515C>T (p.Pro505=) | ClinVar dbSNP COSMIC |
7 | g.55181325delinsAACCCCT | CA645561602 | EGFR,EGFR-AS1 | c.2157delinsAACCCCT (p.Pro719_His720insThrPro) c.665delinsAACCCCT c.2316delinsAACCCCT (p.Pro772_His773insThrPro) c.*28+8397delinsAACCCCT (n.*28+8397delinsAACCCCT) c.2181delinsAACCCCT (p.Pro727_His728insThrPro) n.1246delinsAGGGGTT c.1515delinsAACCCCT (p.Pro505_His506insThrPro) | dbSNP COSMIC |
7 | g.55181328_55181329insAACCAC | CA645561601 | EGFR,EGFR-AS1 | c.2160_2161insAACCAC (p.His720_Val721insAsnHis) c.668_669insAACCAC c.2319_2320insAACCAC (p.His773_Val774insAsnHis) c.*28+8400_*28+8401insAACCAC (n.*28+8400_*28+8401insAACCAC) c.2184_2185insAACCAC (p.His728_Val729insAsnHis) n.1246_1247insTTGTGG c.1518_1519insAACCAC (p.His506_Val507insAsnHis) | dbSNP COSMIC |
7 | g.55181326_55181328dup | CA135866 | EGFR,EGFR-AS1 | c.2158_2160dup (p.His720_Val721insHis) c.666_668dup c.2317_2319dup (p.His773_Val774insHis) c.*28+8398_*28+8400dup (n.*28+8398_*28+8400dup) c.2182_2184dup (p.His728_Val729insHis) n.1244_1246dup c.1516_1518dup (p.His506_Val507insHis) | ClinVar dbSNP COSMIC |
7 | g.55181329_55181330insGCCACG | CA135872 | EGFR,EGFR-AS1 | c.2161_2162insGCCACG (p.His720_Val721insGlyHis) c.669_670insGCCACG c.2320_2321insGCCACG (p.His773_Val774insGlyHis) c.*28+8401_*28+8402insGCCACG (n.*28+8401_*28+8402insGCCACG) c.2185_2186insGCCACG (p.His728_Val729insGlyHis) n.1246_1247insCCGTGG c.1519_1520insGCCACG (p.His506_Val507insGlyHis) | ClinVar dbSNP |
7 | g.55181325_55181330dup | CA645561600 | EGFR,EGFR-AS1 | c.2157_2162dup (p.Val721_Cys722insHisVal) c.665_670dup c.2316_2321dup (p.Val774_Cys775insHisVal) c.*28+8397_*28+8402dup (n.*28+8397_*28+8402dup) c.2181_2186dup (p.Val729_Cys730insHisVal) n.1241_1246dup c.1515_1520dup (p.Val507_Cys508insHisVal) | dbSNP COSMIC COSMIC |
7 | g.55181335_55181336insACCACGTGTGCC | CA2714933682 | EGFR,EGFR-AS1 | c.2167_2168insACCACGTGTGCC (p.Cys722_Arg723insHisHisValCys) c.675_676insACCACGTGTGCC c.2326_2327insACCACGTGTGCC (p.Cys775_Arg776insHisHisValCys) c.*28+8407_*28+8408insACCACGTGTGCC (n.*28+8407_*28+8408insACCACGTGTGCC) c.2191_2192insACCACGTGTGCC (p.Cys730_Arg731insHisHisValCys) n.1246_1247insTGGCACACGTGG c.1525_1526insACCACGTGTGCC (p.Cys508_Arg509insHisHisValCys) | dbSNP |
7 | g.55181327_55181338dup | CA2714933699 | EGFR,EGFR-AS1 | c.2159_2170dup (p.Arg723_Leu724insHisValCysArg) c.667_678dup c.2318_2329dup (p.Arg776_Leu777insHisValCysArg) c.*28+8399_*28+8410dup (n.*28+8399_*28+8410dup) c.2183_2194dup (p.Arg731_Leu732insHisValCysArg) n.1235_1246dup c.1517_1528dup (p.Arg509_Leu510insHisValCysArg) | dbSNP |
7 | g.55181325_55181326insGTT | CA645561603 | EGFR,EGFR-AS1 | c.2157_2158insGTT (p.Pro719_His720insVal) c.665_666insGTT c.2316_2317insGTT (p.Pro772_His773insVal) c.*28+8397_*28+8398insGTT (n.*28+8397_*28+8398insGTT) c.2181_2182insGTT (p.Pro727_His728insVal) n.1245_1246insAAC c.1515_1516insGTT (p.Pro505_His506insVal) | dbSNP COSMIC |
7 | g.55181326C>A | CA367578702 | EGFR,EGFR-AS1 | c.2158C>A (p.His720Asn) c.666C>A c.2317C>A (p.His773Asn) c.*28+8398C>A (n.*28+8398C>A) c.2182C>A (p.His728Asn) n.1245G>T c.1516C>A (p.His506Asn) | gnomAD v4 |
7 | g.55181326C= | CA1708905299 | EGFR,EGFR-AS1 | c.2158C= (p.His720=) c.666C= c.2317C= (p.His773=) c.*28+8398C= (n.*28+8398C=) c.2182C= (p.His728=) n.1245G= c.1516C= (p.His506=) | |
7 | g.55181326C>G | CA158928422 | EGFR,EGFR-AS1 | c.2158C>G (p.His720Asp) c.666C>G c.2317C>G (p.His773Asp) c.*28+8398C>G (n.*28+8398C>G) c.2182C>G (p.His728Asp) n.1245G>C c.1516C>G (p.His506Asp) | ClinVar dbSNP gnomAD v4 |
7 | g.55181326C>T | CA367578699 | EGFR,EGFR-AS1 | c.2158C>T (p.His720Tyr) c.666C>T c.2317C>T (p.His773Tyr) c.*28+8398C>T (n.*28+8398C>T) c.2182C>T (p.His728Tyr) n.1245G>A c.1516C>T (p.His506Tyr) | ClinVar dbSNP gnomAD v4 COSMIC |
7 | g.55181326delinsAACCCCT | CA2580617625 | EGFR,EGFR-AS1 | c.2158delinsAACCCCT (p.His720delinsAsnProTyr) c.666delinsAACCCCT c.2317delinsAACCCCT (p.His773delinsAsnProTyr) c.*28+8398delinsAACCCCT (n.*28+8398delinsAACCCCT) c.2182delinsAACCCCT (p.His728delinsAsnProTyr) n.1245delinsAGGGGTT c.1516delinsAACCCCT (p.His506delinsAsnProTyr) | ClinVar |
7 | g.55181326_55181331dup | CA135869 | EGFR,EGFR-AS1 | c.2158_2163dup (p.Val721_Cys722insHisVal) c.666_671dup c.2317_2322dup (p.Val774_Cys775insHisVal) c.*28+8398_*28+8403dup (n.*28+8398_*28+8403dup) c.2182_2187dup (p.Val729_Cys730insHisVal) n.1240_1245dup c.1516_1521dup (p.Val507_Cys508insHisVal) | ClinVar dbSNP COSMIC COSMIC |
7 | g.55181335_55181336insCACACGTGTGCC | CA2714933715 | EGFR,EGFR-AS1 | c.2167_2168insCACACGTGTGCC (p.Cys722_Arg723insProHisValCys) c.675_676insCACACGTGTGCC c.2326_2327insCACACGTGTGCC (p.Cys775_Arg776insProHisValCys) c.*28+8407_*28+8408insCACACGTGTGCC (n.*28+8407_*28+8408insCACACGTGTGCC) c.2191_2192insCACACGTGTGCC (p.Cys730_Arg731insProHisValCys) n.1245_1246insTGGGCACACGTG c.1525_1526insCACACGTGTGCC (p.Cys508_Arg509insProHisValCys) | dbSNP |
7 | g.55181335_55181336insCGCACGTGTGCC | CA2714933714 | EGFR,EGFR-AS1 | c.2167_2168insCGCACGTGTGCC (p.Cys722_Arg723insProHisValCys) c.675_676insCGCACGTGTGCC c.2326_2327insCGCACGTGTGCC (p.Cys775_Arg776insProHisValCys) c.*28+8407_*28+8408insCGCACGTGTGCC (n.*28+8407_*28+8408insCGCACGTGTGCC) c.2191_2192insCGCACGTGTGCC (p.Cys730_Arg731insProHisValCys) n.1245_1246insCGGGCACACGTG c.1525_1526insCGCACGTGTGCC (p.Cys508_Arg509insProHisValCys) | dbSNP |
7 | g.55181335_55181336insCTCACGTGTGCC | CA2714934246 | EGFR,EGFR-AS1 | c.2167_2168insCTCACGTGTGCC (p.Cys722_Arg723insProHisValCys) c.675_676insCTCACGTGTGCC c.2326_2327insCTCACGTGTGCC (p.Cys775_Arg776insProHisValCys) c.*28+8407_*28+8408insCTCACGTGTGCC (n.*28+8407_*28+8408insCTCACGTGTGCC) c.2191_2192insCTCACGTGTGCC (p.Cys730_Arg731insProHisValCys) n.1245_1246insAGGGCACACGTG c.1525_1526insCTCACGTGTGCC (p.Cys508_Arg509insProHisValCys) | dbSNP |
7 | g.55181326_55181327insCTAACCCCT | CA645561604 | EGFR,EGFR-AS1 | c.2158_2159insCTAACCCCT (p.His720delinsProAsnProTyr) c.666_667insCTAACCCCT c.2317_2318insCTAACCCCT (p.His773delinsProAsnProTyr) c.*28+8398_*28+8399insCTAACCCCT (n.*28+8398_*28+8399insCTAACCCCT) c.2182_2183insCTAACCCCT (p.His728delinsProAsnProTyr) n.1244_1245insAGGGGTTAG c.1516_1517insCTAACCCCT (p.His506delinsProAsnProTyr) | dbSNP COSMIC |
7 | g.55181327A= | CA1708905310 | EGFR,EGFR-AS1 | c.2159A= (p.His720=) c.667A= c.2318A= (p.His773=) c.*28+8399A= (n.*28+8399A=) c.2183A= (p.His728=) n.1244T= c.1517A= (p.His506=) | |
7 | g.55181327A>C | CA367578708 | EGFR,EGFR-AS1 | c.2159A>C (p.His720Pro) c.667A>C c.2318A>C (p.His773Pro) c.*28+8399A>C (n.*28+8399A>C) c.2183A>C (p.His728Pro) n.1244T>G c.1517A>C (p.His506Pro) | dbSNP COSMIC |
7 | g.55181327A>G | CA16602544 | EGFR,EGFR-AS1 | c.2159A>G (p.His720Arg) c.667A>G c.2318A>G (p.His773Arg) c.*28+8399A>G (n.*28+8399A>G) c.2183A>G (p.His728Arg) n.1244T>C c.1517A>G (p.His506Arg) | ClinVar dbSNP COSMIC |
7 | g.55181327A>T | CA367578706 | EGFR,EGFR-AS1 | c.2159A>T (p.His720Leu) c.667A>T c.2318A>T (p.His773Leu) c.*28+8399A>T (n.*28+8399A>T) c.2183A>T (p.His728Leu) n.1244T>A c.1517A>T (p.His506Leu) | dbSNP COSMIC |
7 | g.55181327_55181329delinsTCA | CA2573320521 | EGFR,EGFR-AS1 | c.2159_2161delinsTCA (p.His720_Val721delinsLeuMet) c.667_669delinsTCA c.2318_2320delinsTCA (p.His773_Val774delinsLeuMet) c.*28+8399_*28+8401delinsTCA (n.*28+8399_*28+8401delinsTCA) c.2183_2185delinsTCA (p.His728_Val729delinsLeuMet) n.1242_1244delinsTGA c.1517_1519delinsTCA (p.His506_Val507delinsLeuMet) | ClinVar |
7 | g.55181335_55181336insCCGACGTGTGCC | CA2714934251 | EGFR,EGFR-AS1 | c.2167_2168insCCGACGTGTGCC (p.Cys722_Arg723insProAspValCys) c.675_676insCCGACGTGTGCC c.2326_2327insCCGACGTGTGCC (p.Cys775_Arg776insProAspValCys) c.*28+8407_*28+8408insCCGACGTGTGCC (n.*28+8407_*28+8408insCCGACGTGTGCC) c.2191_2192insCCGACGTGTGCC (p.Cys730_Arg731insProAspValCys) n.1244_1245insCGGGGCACACGT c.1525_1526insCCGACGTGTGCC (p.Cys508_Arg509insProAspValCys) | dbSNP |
7 | g.55181328C>A | CA367578713 | EGFR,EGFR-AS1 | c.2160C>A (p.His720Gln) c.668C>A c.2319C>A (p.His773Gln) c.*28+8400C>A (n.*28+8400C>A) c.2184C>A (p.His728Gln) n.1243G>T c.1518C>A (p.His506Gln) | dbSNP gnomAD v4 |
7 | g.55181328C= | CA1708905319 | EGFR,EGFR-AS1 | c.2160C= (p.His720=) c.668C= c.2319C= (p.His773=) c.*28+8400C= (n.*28+8400C=) c.2184C= (p.His728=) n.1243G= c.1518C= (p.His506=) | |
7 | g.55181328C>G | CA367578711 | EGFR,EGFR-AS1 | c.2160C>G (p.His720Gln) c.668C>G c.2319C>G (p.His773Gln) c.*28+8400C>G (n.*28+8400C>G) c.2184C>G (p.His728Gln) n.1243G>C c.1518C>G (p.His506Gln) | dbSNP gnomAD v2 gnomAD v4 |
7 | g.55181328C>T | CA4266054 | EGFR,EGFR-AS1 | c.2160C>T (p.His720=) c.668C>T c.2319C>T (p.His773=) c.*28+8400C>T (n.*28+8400C>T) c.2184C>T (p.His728=) n.1243G>A c.1518C>T (p.His506=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.55181328_55181329insACACAACCCCCC | CA645561605 | EGFR,EGFR-AS1 | c.2160_2161insACACAACCCCCC (p.His720_Val721insThrGlnProPro) c.668_669insACACAACCCCCC c.2319_2320insACACAACCCCCC (p.His773_Val774insThrGlnProPro) c.*28+8400_*28+8401insACACAACCCCCC (n.*28+8400_*28+8401insACACAACCCCCC) c.2184_2185insACACAACCCCCC (p.His728_Val729insThrGlnProPro) n.1243_1244insGGGGGTTGTGTG c.1518_1519insACACAACCCCCC (p.His506_Val507insThrGlnProPro) | dbSNP COSMIC |
7 | g.55181335_55181336insCCCCCGTGTGCC | CA2714934260 | EGFR,EGFR-AS1 | c.2167_2168insCCCCCGTGTGCC (p.Cys722_Arg723insProProValCys) c.675_676insCCCCCGTGTGCC c.2326_2327insCCCCCGTGTGCC (p.Cys775_Arg776insProProValCys) c.*28+8407_*28+8408insCCCCCGTGTGCC (n.*28+8407_*28+8408insCCCCCGTGTGCC) c.2191_2192insCCCCCGTGTGCC (p.Cys730_Arg731insProProValCys) n.1243_1244insGGGGGGCACACG c.1525_1526insCCCCCGTGTGCC (p.Cys508_Arg509insProProValCys) | dbSNP |
7 | g.55181335_55181336insCCCGCGTGTGCC | CA2714934257 | EGFR,EGFR-AS1 | c.2167_2168insCCCGCGTGTGCC (p.Cys722_Arg723insProArgValCys) c.675_676insCCCGCGTGTGCC c.2326_2327insCCCGCGTGTGCC (p.Cys775_Arg776insProArgValCys) c.*28+8407_*28+8408insCCCGCGTGTGCC (n.*28+8407_*28+8408insCCCGCGTGTGCC) c.2191_2192insCCCGCGTGTGCC (p.Cys730_Arg731insProArgValCys) n.1243_1244insCGGGGGCACACG c.1525_1526insCCCGCGTGTGCC (p.Cys508_Arg509insProArgValCys) | dbSNP |
7 | g.55181335_55181336insCCCTCGTGTGCC | CA2714934255 | EGFR,EGFR-AS1 | c.2167_2168insCCCTCGTGTGCC (p.Cys722_Arg723insProLeuValCys) c.675_676insCCCTCGTGTGCC c.2326_2327insCCCTCGTGTGCC (p.Cys775_Arg776insProLeuValCys) c.*28+8407_*28+8408insCCCTCGTGTGCC (n.*28+8407_*28+8408insCCCTCGTGTGCC) c.2191_2192insCCCTCGTGTGCC (p.Cys730_Arg731insProLeuValCys) n.1243_1244insAGGGGGCACACG c.1525_1526insCCCTCGTGTGCC (p.Cys508_Arg509insProLeuValCys) | dbSNP |
7 | g.55181328_55181329insCAG | CA645561606 | EGFR,EGFR-AS1 | c.2160_2161insCAG (p.His720_Val721insGln) c.668_669insCAG c.2319_2320insCAG (p.His773_Val774insGln) c.*28+8400_*28+8401insCAG (n.*28+8400_*28+8401insCAG) c.2184_2185insCAG (p.His728_Val729insGln) n.1242_1243insCTG c.1518_1519insCAG (p.His506_Val507insGln) | dbSNP COSMIC |
7 | g.55181329G>A | CA158928427 | EGFR,EGFR-AS1 | c.2161G>A (p.Val721Met) c.669G>A c.2320G>A (p.Val774Met) c.*28+8401G>A (n.*28+8401G>A) c.2185G>A (p.Val729Met) n.1242C>T c.1519G>A (p.Val507Met) | ClinVar dbSNP gnomAD v2 gnomAD v4 COSMIC |
7 | g.55181329G>C | CA158928432 | EGFR,EGFR-AS1 | c.2161G>C (p.Val721Leu) c.669G>C c.2320G>C (p.Val774Leu) c.*28+8401G>C (n.*28+8401G>C) c.2185G>C (p.Val729Leu) n.1242C>G c.1519G>C (p.Val507Leu) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.55181329G= | CA1708905326 | EGFR,EGFR-AS1 | c.2161G= (p.Val721=) c.669G= c.2320G= (p.Val774=) c.*28+8401G= (n.*28+8401G=) c.2185G= (p.Val729=) n.1242C= c.1519G= (p.Val507=) | |
7 | g.55181329G>T | CA367578717 | EGFR,EGFR-AS1 | c.2161G>T (p.Val721Leu) c.669G>T c.2320G>T (p.Val774Leu) c.*28+8401G>T (n.*28+8401G>T) c.2185G>T (p.Val729Leu) n.1242C>A c.1519G>T (p.Val507Leu) | COSMIC |
7 | g.55181335_55181336insCCCAGGTGTGCC | CA2714934269 | EGFR,EGFR-AS1 | c.2167_2168insCCCAGGTGTGCC (p.Cys722_Arg723insProGlnValCys) c.675_676insCCCAGGTGTGCC c.2326_2327insCCCAGGTGTGCC (p.Cys775_Arg776insProGlnValCys) c.*28+8407_*28+8408insCCCAGGTGTGCC (n.*28+8407_*28+8408insCCCAGGTGTGCC) c.2191_2192insCCCAGGTGTGCC (p.Cys730_Arg731insProGlnValCys) n.1242_1243insCTGGGGGCACAC c.1525_1526insCCCAGGTGTGCC (p.Cys508_Arg509insProGlnValCys) | dbSNP |
7 | g.55181330T>A | CA367578720 | EGFR,EGFR-AS1 | c.2162T>A (p.Val721Glu) c.670T>A c.2321T>A (p.Val774Glu) c.*28+8402T>A (n.*28+8402T>A) c.2186T>A (p.Val729Glu) n.1241A>T c.1520T>A (p.Val507Glu) | dbSNP |
7 | g.55181330T>C | CA367578723 | EGFR,EGFR-AS1 | c.2162T>C (p.Val721Ala) c.670T>C c.2321T>C (p.Val774Ala) c.*28+8402T>C (n.*28+8402T>C) c.2186T>C (p.Val729Ala) n.1241A>G c.1520T>C (p.Val507Ala) | |
7 | g.55181330T>G | CA367578724 | EGFR,EGFR-AS1 | c.2162T>G (p.Val721Gly) c.670T>G c.2321T>G (p.Val774Gly) c.*28+8402T>G (n.*28+8402T>G) c.2186T>G (p.Val729Gly) n.1241A>C c.1520T>G (p.Val507Gly) | |
7 | g.55181335_55181336insCCCACATGTGCC | CA2714934289 | EGFR,EGFR-AS1 | c.2167_2168insCCCACATGTGCC (p.Cys722_Arg723insProHisMetCys) c.675_676insCCCACATGTGCC c.2326_2327insCCCACATGTGCC (p.Cys775_Arg776insProHisMetCys) c.*28+8407_*28+8408insCCCACATGTGCC (n.*28+8407_*28+8408insCCCACATGTGCC) c.2191_2192insCCCACATGTGCC (p.Cys730_Arg731insProHisMetCys) n.1241_1242insTGTGGGGGCACA c.1525_1526insCCCACATGTGCC (p.Cys508_Arg509insProHisMetCys) | dbSNP |
7 | g.55181335_55181336insCCCACCTGTGCC | CA2714934378 | EGFR,EGFR-AS1 | c.2167_2168insCCCACCTGTGCC (p.Cys722_Arg723insProHisLeuCys) c.675_676insCCCACCTGTGCC c.2326_2327insCCCACCTGTGCC (p.Cys775_Arg776insProHisLeuCys) c.*28+8407_*28+8408insCCCACCTGTGCC (n.*28+8407_*28+8408insCCCACCTGTGCC) c.2191_2192insCCCACCTGTGCC (p.Cys730_Arg731insProHisLeuCys) n.1241_1242insGGTGGGGGCACA c.1525_1526insCCCACCTGTGCC (p.Cys508_Arg509insProHisLeuCys) | dbSNP |
7 | g.55181335_55181336insCCCCCCTGTGCC | CA2714934402 | EGFR,EGFR-AS1 | c.2167_2168insCCCCCCTGTGCC (p.Cys722_Arg723insProProLeuCys) c.675_676insCCCCCCTGTGCC c.2326_2327insCCCCCCTGTGCC (p.Cys775_Arg776insProProLeuCys) c.*28+8407_*28+8408insCCCCCCTGTGCC (n.*28+8407_*28+8408insCCCCCCTGTGCC) c.2191_2192insCCCCCCTGTGCC (p.Cys730_Arg731insProProLeuCys) n.1241_1242insGGGGGGGGCACA c.1525_1526insCCCCCCTGTGCC (p.Cys508_Arg509insProProLeuCys) | dbSNP |
7 | g.55181331G>A | CA455165092 | EGFR,EGFR-AS1 | c.2163G>A (p.Val721=) c.671G>A c.2322G>A (p.Val774=) c.*28+8403G>A (n.*28+8403G>A) c.2187G>A (p.Val729=) n.1240C>T c.1521G>A (p.Val507=) | ClinVar dbSNP gnomAD v4 |
7 | g.55181331G>C | CA455165094 | EGFR,EGFR-AS1 | c.2163G>C (p.Val721=) c.671G>C c.2322G>C (p.Val774=) c.*28+8403G>C (n.*28+8403G>C) c.2187G>C (p.Val729=) n.1240C>G c.1521G>C (p.Val507=) | |
7 | g.55181331G>T | CA455165093 | EGFR,EGFR-AS1 | c.2163G>T (p.Val721=) c.671G>T c.2322G>T (p.Val774=) c.*28+8403G>T (n.*28+8403G>T) c.2187G>T (p.Val729=) n.1240C>A c.1521G>T (p.Val507=) | |
7 | g.55181335_55181336insCCCACGAGTGCC | CA2714934439 | EGFR,EGFR-AS1 | c.2167_2168insCCCACGAGTGCC (p.Cys722_Arg723insProHisGluCys) c.675_676insCCCACGAGTGCC c.2326_2327insCCCACGAGTGCC (p.Cys775_Arg776insProHisGluCys) c.*28+8407_*28+8408insCCCACGAGTGCC (n.*28+8407_*28+8408insCCCACGAGTGCC) c.2191_2192insCCCACGAGTGCC (p.Cys730_Arg731insProHisGluCys) n.1240_1241insTCGTGGGGGCAC c.1525_1526insCCCACGAGTGCC (p.Cys508_Arg509insProHisGluCys) | dbSNP |
7 | g.55181335_55181336insCCCACGCGTGCC | CA2714934452 | EGFR,EGFR-AS1 | c.2167_2168insCCCACGCGTGCC (p.Cys722_Arg723insProHisAlaCys) c.675_676insCCCACGCGTGCC c.2326_2327insCCCACGCGTGCC (p.Cys775_Arg776insProHisAlaCys) c.*28+8407_*28+8408insCCCACGCGTGCC (n.*28+8407_*28+8408insCCCACGCGTGCC) c.2191_2192insCCCACGCGTGCC (p.Cys730_Arg731insProHisAlaCys) n.1240_1241insGCGTGGGGGCAC c.1525_1526insCCCACGCGTGCC (p.Cys508_Arg509insProHisAlaCys) | dbSNP |
7 | g.55181331_55181332insCATGTT | CA2573051288 | EGFR,EGFR-AS1 | c.2163_2164insCATGTT (p.Val721_Cys722insHisVal) c.671_672insCATGTT c.2322_2323insCATGTT (p.Val774_Cys775insHisVal) c.*28+8403_*28+8404insCATGTT (n.*28+8403_*28+8404insCATGTT) c.2187_2188insCATGTT (p.Val729_Cys730insHisVal) n.1239_1240insAACATG c.1521_1522insCATGTT (p.Val507_Cys508insHisVal) | |
7 | g.55181331_55181332insCCACGT | CA645561607 | EGFR,EGFR-AS1 | c.2163_2164insCCACGT (p.Val721_Cys722insProArg) c.671_672insCCACGT c.2322_2323insCCACGT (p.Val774_Cys775insProArg) c.*28+8403_*28+8404insCCACGT (n.*28+8403_*28+8404insCCACGT) c.2187_2188insCCACGT (p.Val729_Cys730insProArg) n.1239_1240insACGTGG c.1521_1522insCCACGT (p.Val507_Cys508insProArg) | dbSNP COSMIC |
7 | g.55181332T>A | CA367578727 | EGFR,EGFR-AS1 | c.2164T>A (p.Cys722Ser) c.672T>A c.2323T>A (p.Cys775Ser) c.*28+8404T>A (n.*28+8404T>A) c.2188T>A (p.Cys730Ser) n.1239A>T c.1522T>A (p.Cys508Ser) | gnomAD v4 |
7 | g.55181332T>C | CA367578729 | EGFR,EGFR-AS1 | c.2164T>C (p.Cys722Arg) c.672T>C c.2323T>C (p.Cys775Arg) c.*28+8404T>C (n.*28+8404T>C) c.2188T>C (p.Cys730Arg) n.1239A>G c.1522T>C (p.Cys508Arg) | |
7 | g.55181332T>G | CA367578731 | EGFR,EGFR-AS1 | c.2164T>G (p.Cys722Gly) c.672T>G c.2323T>G (p.Cys775Gly) c.*28+8404T>G (n.*28+8404T>G) c.2188T>G (p.Cys730Gly) n.1239A>C c.1522T>G (p.Cys508Gly) | gnomAD v4 |
7 | g.55181333G>A | CA367578734 | EGFR,EGFR-AS1 | c.2165G>A (p.Cys722Tyr) c.673G>A c.2324G>A (p.Cys775Tyr) c.*28+8405G>A (n.*28+8405G>A) c.2189G>A (p.Cys730Tyr) n.1238C>T c.1523G>A (p.Cys508Tyr) | ClinVar dbSNP COSMIC |
7 | g.55181333G>C | CA367578736 | EGFR,EGFR-AS1 | c.2165G>C (p.Cys722Ser) c.673G>C c.2324G>C (p.Cys775Ser) c.*28+8405G>C (n.*28+8405G>C) c.2189G>C (p.Cys730Ser) n.1238C>G c.1523G>C (p.Cys508Ser) | |
7 | g.55181333G>T | CA367578738 | EGFR,EGFR-AS1 | c.2165G>T (p.Cys722Phe) c.673G>T c.2324G>T (p.Cys775Phe) c.*28+8405G>T (n.*28+8405G>T) c.2189G>T (p.Cys730Phe) n.1238C>A c.1523G>T (p.Cys508Phe) | dbSNP |
7 | g.55181335_55181336insCCCACGGGGGCC | CA2714934789 | EGFR,EGFR-AS1 | c.2167_2168insCCCACGGGGGCC (p.Cys722_Arg723insProHisGlyGly) c.675_676insCCCACGGGGGCC c.2326_2327insCCCACGGGGGCC (p.Cys775_Arg776insProHisGlyGly) c.*28+8407_*28+8408insCCCACGGGGGCC (n.*28+8407_*28+8408insCCCACGGGGGCC) c.2191_2192insCCCACGGGGGCC (p.Cys730_Arg731insProHisGlyGly) n.1238_1239insCCCCGTGGGGGC c.1525_1526insCCCACGGGGGCC (p.Cys508_Arg509insProHisGlyGly) | dbSNP |
7 | g.55181335_55181336insCCCACGTGCGCC | CA2714934830 | EGFR,EGFR-AS1 | c.2167_2168insCCCACGTGCGCC (p.Cys722_Arg723insProHisValArg) c.675_676insCCCACGTGCGCC c.2326_2327insCCCACGTGCGCC (p.Cys775_Arg776insProHisValArg) c.*28+8407_*28+8408insCCCACGTGCGCC (n.*28+8407_*28+8408insCCCACGTGCGCC) c.2191_2192insCCCACGTGCGCC (p.Cys730_Arg731insProHisValArg) n.1238_1239insGCACGTGGGGGC c.1525_1526insCCCACGTGCGCC (p.Cys508_Arg509insProHisValArg) | dbSNP |
7 | g.55181335_55181336insCCCACGTGGGCC | CA2714934798 | EGFR,EGFR-AS1 | c.2167_2168insCCCACGTGGGCC (p.Cys722_Arg723insProHisValGly) c.675_676insCCCACGTGGGCC c.2326_2327insCCCACGTGGGCC (p.Cys775_Arg776insProHisValGly) c.*28+8407_*28+8408insCCCACGTGGGCC (n.*28+8407_*28+8408insCCCACGTGGGCC) c.2191_2192insCCCACGTGGGCC (p.Cys730_Arg731insProHisValGly) n.1238_1239insCCACGTGGGGGC c.1525_1526insCCCACGTGGGCC (p.Cys508_Arg509insProHisValGly) | dbSNP |
7 | g.55181335_55181336insCCCAGGTGGGCC | CA2714934796 | EGFR,EGFR-AS1 | c.2167_2168insCCCAGGTGGGCC (p.Cys722_Arg723insProGlnValGly) c.675_676insCCCAGGTGGGCC c.2326_2327insCCCAGGTGGGCC (p.Cys775_Arg776insProGlnValGly) c.*28+8407_*28+8408insCCCAGGTGGGCC (n.*28+8407_*28+8408insCCCAGGTGGGCC) c.2191_2192insCCCAGGTGGGCC (p.Cys730_Arg731insProGlnValGly) n.1238_1239insCCACCTGGGGGC c.1525_1526insCCCAGGTGGGCC (p.Cys508_Arg509insProGlnValGly) | dbSNP |
7 | g.55181334C>A | CA367578742 | EGFR,EGFR-AS1 | c.2166C>A (p.Cys722Ter) c.674C>A c.2325C>A (p.Cys775Ter) c.*28+8406C>A (n.*28+8406C>A) c.2190C>A (p.Cys730Ter) n.1237G>T c.1524C>A (p.Cys508Ter) | |
7 | g.55181334C>G | CA367578740 | EGFR,EGFR-AS1 | c.2166C>G (p.Cys722Trp) c.674C>G c.2325C>G (p.Cys775Trp) c.*28+8406C>G (n.*28+8406C>G) c.2190C>G (p.Cys730Trp) n.1237G>C c.1524C>G (p.Cys508Trp) | |
7 | g.55181334C>T | CA455165096 | EGFR,EGFR-AS1 | c.2166C>T (p.Cys722=) c.674C>T c.2325C>T (p.Cys775=) c.*28+8406C>T (n.*28+8406C>T) c.2190C>T (p.Cys730=) n.1237G>A c.1524C>T (p.Cys508=) | ClinVar dbSNP |
7 | g.55181335_55181336insCCCACGTGTTCC | CA2714934841 | EGFR,EGFR-AS1 | c.2167_2168insCCCACGTGTTCC (p.Cys722_Arg723insProHisValPhe) c.675_676insCCCACGTGTTCC c.2326_2327insCCCACGTGTTCC (p.Cys775_Arg776insProHisValPhe) c.*28+8407_*28+8408insCCCACGTGTTCC (n.*28+8407_*28+8408insCCCACGTGTTCC) c.2191_2192insCCCACGTGTTCC (p.Cys730_Arg731insProHisValPhe) n.1237_1238insAACACGTGGGGG c.1525_1526insCCCACGTGTTCC (p.Cys508_Arg509insProHisValPhe) | dbSNP |
7 | g.55181335_55181336insCCCCCGTGTCCC | CA2714935170 | EGFR,EGFR-AS1 | c.2167_2168insCCCCCGTGTCCC (p.Cys722_Arg723insProProValSer) c.675_676insCCCCCGTGTCCC c.2326_2327insCCCCCGTGTCCC (p.Cys775_Arg776insProProValSer) c.*28+8407_*28+8408insCCCCCGTGTCCC (n.*28+8407_*28+8408insCCCCCGTGTCCC) c.2191_2192insCCCCCGTGTCCC (p.Cys730_Arg731insProProValSer) n.1237_1238insGACACGGGGGGG c.1525_1526insCCCCCGTGTCCC (p.Cys508_Arg509insProProValSer) | dbSNP |
7 | g.55181335_55181336insCCCTCGTGTCCC | CA2714935171 | EGFR,EGFR-AS1 | c.2167_2168insCCCTCGTGTCCC (p.Cys722_Arg723insProLeuValSer) c.675_676insCCCTCGTGTCCC c.2326_2327insCCCTCGTGTCCC (p.Cys775_Arg776insProLeuValSer) c.*28+8407_*28+8408insCCCTCGTGTCCC (n.*28+8407_*28+8408insCCCTCGTGTCCC) c.2191_2192insCCCTCGTGTCCC (p.Cys730_Arg731insProLeuValSer) n.1237_1238insGACACGAGGGGG c.1525_1526insCCCTCGTGTCCC (p.Cys508_Arg509insProLeuValSer) | dbSNP |
7 | g.55181335_55181336insCCGACGTGTCCC | CA2714935199 | EGFR,EGFR-AS1 | c.2167_2168insCCGACGTGTCCC (p.Cys722_Arg723insProAspValSer) c.675_676insCCGACGTGTCCC c.2326_2327insCCGACGTGTCCC (p.Cys775_Arg776insProAspValSer) c.*28+8407_*28+8408insCCGACGTGTCCC (n.*28+8407_*28+8408insCCGACGTGTCCC) c.2191_2192insCCGACGTGTCCC (p.Cys730_Arg731insProAspValSer) n.1237_1238insGACACGTCGGGG c.1525_1526insCCGACGTGTCCC (p.Cys508_Arg509insProAspValSer) | dbSNP |
7 | g.55181335C>A | CA367578745 | EGFR,EGFR-AS1 | c.2167C>A (p.Arg723Ser) c.675C>A c.2326C>A (p.Arg776Ser) c.*28+8407C>A (n.*28+8407C>A) c.2191C>A (p.Arg731Ser) n.1236G>T c.1525C>A (p.Arg509Ser) | dbSNP COSMIC |
7 | g.55181335C= | CA1708905330 | EGFR,EGFR-AS1 | c.2167C= (p.Arg723=) c.675C= c.2326C= (p.Arg776=) c.*28+8407C= (n.*28+8407C=) c.2191C= (p.Arg731=) n.1236G= c.1525C= (p.Arg509=) | |
7 | g.55181335C>G | CA367578746 | EGFR,EGFR-AS1 | c.2167C>G (p.Arg723Gly) c.675C>G c.2326C>G (p.Arg776Gly) c.*28+8407C>G (n.*28+8407C>G) c.2191C>G (p.Arg731Gly) n.1236G>C c.1525C>G (p.Arg509Gly) | dbSNP |
7 | g.55181335C>T | CA367578749 | EGFR,EGFR-AS1 | c.2167C>T (p.Arg723Cys) c.675C>T c.2326C>T (p.Arg776Cys) c.*28+8407C>T (n.*28+8407C>T) c.2191C>T (p.Arg731Cys) n.1236G>A c.1525C>T (p.Arg509Cys) | ClinVar dbSNP gnomAD v3 gnomAD v4 COSMIC |
7 | g.55181335_55181336insCCCACGTGTGTC | CA2714935210 | EGFR,EGFR-AS1 | c.2167_2168insCCCACGTGTGTC (p.Cys722_Arg723insProHisValCys) c.675_676insCCCACGTGTGTC c.2326_2327insCCCACGTGTGTC (p.Cys775_Arg776insProHisValCys) c.*28+8407_*28+8408insCCCACGTGTGTC (n.*28+8407_*28+8408insCCCACGTGTGTC) c.2191_2192insCCCACGTGTGTC (p.Cys730_Arg731insProHisValCys) n.1236_1237insACACACGTGGGG c.1525_1526insCCCACGTGTGTC (p.Cys508_Arg509insProHisValCys) | dbSNP |
7 | g.55181335_55181336insCCCACGTGTGCA | CA2714935250 | EGFR,EGFR-AS1 | c.2167_2168insCCCACGTGTGCA (p.Arg723delinsProHisValCysSer) c.675_676insCCCACGTGTGCA c.2326_2327insCCCACGTGTGCA (p.Arg776delinsProHisValCysSer) c.*28+8407_*28+8408insCCCACGTGTGCA (n.*28+8407_*28+8408insCCCACGTGTGCA) c.2191_2192insCCCACGTGTGCA (p.Arg731delinsProHisValCysSer) n.1235_1236insTGCACACGTGGG c.1525_1526insCCCACGTGTGCA (p.Arg509delinsProHisValCysSer) | dbSNP |
7 | g.55181335_55181336insCCCACGTGTGCG | CA2714935218 | EGFR,EGFR-AS1 | c.2167_2168insCCCACGTGTGCG (p.Arg723delinsProHisValCysGly) c.675_676insCCCACGTGTGCG c.2326_2327insCCCACGTGTGCG (p.Arg776delinsProHisValCysGly) c.*28+8407_*28+8408insCCCACGTGTGCG (n.*28+8407_*28+8408insCCCACGTGTGCG) c.2191_2192insCCCACGTGTGCG (p.Arg731delinsProHisValCysGly) n.1235_1236insCGCACACGTGGG c.1525_1526insCCCACGTGTGCG (p.Arg509delinsProHisValCysGly) | dbSNP |
7 | g.55181336G>A | CA151166 | EGFR,EGFR-AS1 | c.2168G>A (p.Arg723His) c.676G>A c.2327G>A (p.Arg776His) c.*28+8408G>A (n.*28+8408G>A) c.2192G>A (p.Arg731His) n.1235C>T c.1526G>A (p.Arg509His) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
7 | g.55181336G>C | CA367578751 | EGFR,EGFR-AS1 | c.2168G>C (p.Arg723Pro) c.676G>C c.2327G>C (p.Arg776Pro) c.*28+8408G>C (n.*28+8408G>C) c.2192G>C (p.Arg731Pro) n.1235C>G c.1526G>C (p.Arg509Pro) | dbSNP |
7 | g.55181336G= | CA1708905335 | EGFR,EGFR-AS1 | c.2168G= (p.Arg723=) c.676G= c.2327G= (p.Arg776=) c.*28+8408G= (n.*28+8408G=) c.2192G= (p.Arg731=) n.1235C= c.1526G= (p.Arg509=) | |
7 | g.55181336G>T | CA367578753 | EGFR,EGFR-AS1 | c.2168G>T (p.Arg723Leu) c.676G>T c.2327G>T (p.Arg776Leu) c.*28+8408G>T (n.*28+8408G>T) c.2192G>T (p.Arg731Leu) n.1235C>A c.1526G>T (p.Arg509Leu) | gnomAD v4 |
7 | g.55181337C>A | CA4266055 | EGFR,EGFR-AS1 | c.2169C>A (p.Arg723=) c.677C>A c.2328C>A (p.Arg776=) c.*28+8409C>A (n.*28+8409C>A) c.2193C>A (p.Arg731=) n.1234G>T c.1527C>A (p.Arg509=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
7 | g.55181337C= | CA1708905344 | EGFR,EGFR-AS1 | c.2169C= (p.Arg723=) c.677C= c.2328C= (p.Arg776=) c.*28+8409C= (n.*28+8409C=) c.2193C= (p.Arg731=) n.1234G= c.1527C= (p.Arg509=) | |
7 | g.55181337C>G | CA158928441 | EGFR,EGFR-AS1 | c.2169C>G (p.Arg723=) c.677C>G c.2328C>G (p.Arg776=) c.*28+8409C>G (n.*28+8409C>G) c.2193C>G (p.Arg731=) n.1234G>C c.1527C>G (p.Arg509=) | dbSNP |
7 | g.55181337C>T | CA455165100 | EGFR,EGFR-AS1 | c.2169C>T (p.Arg723=) c.677C>T c.2328C>T (p.Arg776=) c.*28+8409C>T (n.*28+8409C>T) c.2193C>T (p.Arg731=) n.1234G>A c.1527C>T (p.Arg509=) | dbSNP |
7 | g.55181338C>A | CA367578756 | EGFR,EGFR-AS1 | c.2170C>A (p.Leu724Met) c.678C>A c.2329C>A (p.Leu777Met) c.*28+8410C>A (n.*28+8410C>A) c.2194C>A (p.Leu732Met) n.1233G>T c.1528C>A (p.Leu510Met) | dbSNP |
7 | g.55181338C= | CA1708905353 | EGFR,EGFR-AS1 | c.2170C= (p.Leu724=) c.678C= c.2329C= (p.Leu777=) c.*28+8410C= (n.*28+8410C=) c.2194C= (p.Leu732=) n.1233G= c.1528C= (p.Leu510=) | |
7 | g.55181338C>G | CA367578757 | EGFR,EGFR-AS1 | c.2170C>G (p.Leu724Val) c.678C>G c.2329C>G (p.Leu777Val) c.*28+8410C>G (n.*28+8410C>G) c.2194C>G (p.Leu732Val) n.1233G>C c.1528C>G (p.Leu510Val) | dbSNP |
7 | g.55181338C>T | CA135875 | EGFR,EGFR-AS1 | c.2170C>T (p.Leu724=) c.678C>T c.2329C>T (p.Leu777=) c.*28+8410C>T (n.*28+8410C>T) c.2194C>T (p.Leu732=) n.1233G>A c.1528C>T (p.Leu510=) | ClinVar dbSNP |
7 | g.55181339T>A | CA367578760 | EGFR,EGFR-AS1 | c.2171T>A (p.Leu724Gln) c.679T>A c.2330T>A (p.Leu777Gln) c.*28+8411T>A (n.*28+8411T>A) c.2195T>A (p.Leu732Gln) n.1232A>T c.1529T>A (p.Leu510Gln) | dbSNP COSMIC |
7 | g.55181339T>C | CA367578762 | EGFR,EGFR-AS1 | c.2171T>C (p.Leu724Pro) c.679T>C c.2330T>C (p.Leu777Pro) c.*28+8411T>C (n.*28+8411T>C) c.2195T>C (p.Leu732Pro) n.1232A>G c.1529T>C (p.Leu510Pro) | dbSNP gnomAD v4 |
7 | g.55181339T>G | CA367578763 | EGFR,EGFR-AS1 | c.2171T>G (p.Leu724Arg) c.679T>G c.2330T>G (p.Leu777Arg) c.*28+8411T>G (n.*28+8411T>G) c.2195T>G (p.Leu732Arg) n.1232A>C c.1529T>G (p.Leu510Arg) | |
7 | g.55181340G>A | CA455165102 | EGFR,EGFR-AS1 | c.2172G>A (p.Leu724=) c.680G>A c.2331G>A (p.Leu777=) c.*28+8412G>A (n.*28+8412G>A) c.2196G>A (p.Leu732=) n.1231C>T c.1530G>A (p.Leu510=) | dbSNP gnomAD v2 gnomAD v4 |
7 | g.55181340G>C | CA455165103 | EGFR,EGFR-AS1 | c.2172G>C (p.Leu724=) c.680G>C c.2331G>C (p.Leu777=) c.*28+8412G>C (n.*28+8412G>C) c.2196G>C (p.Leu732=) n.1231C>G c.1530G>C (p.Leu510=) | dbSNP |
7 | g.55181340G= | CA1708905357 | EGFR,EGFR-AS1 | c.2172G= (p.Leu724=) c.680G= c.2331G= (p.Leu777=) c.*28+8412G= (n.*28+8412G=) c.2196G= (p.Leu732=) n.1231C= c.1530G= (p.Leu510=) | |
7 | g.55181340G>T | CA455165105 | EGFR,EGFR-AS1 | c.2172G>T (p.Leu724=) c.680G>T c.2331G>T (p.Leu777=) c.*28+8412G>T (n.*28+8412G>T) c.2196G>T (p.Leu732=) n.1231C>A c.1530G>T (p.Leu510=) | |
7 | g.55181341C>A | CA367578766 | EGFR,EGFR-AS1 | c.2173C>A (p.Leu725Met) c.681C>A c.2332C>A (p.Leu778Met) c.*28+8413C>A (n.*28+8413C>A) c.2197C>A (p.Leu733Met) n.1230G>T c.1531C>A (p.Leu511Met) | |
7 | g.55181341C>G | CA367578768 | EGFR,EGFR-AS1 | c.2173C>G (p.Leu725Val) c.681C>G c.2332C>G (p.Leu778Val) c.*28+8413C>G (n.*28+8413C>G) c.2197C>G (p.Leu733Val) n.1230G>C c.1531C>G (p.Leu511Val) | dbSNP |
7 | g.55181341C>T | CA455165108 | EGFR,EGFR-AS1 | c.2173C>T (p.Leu725=) c.681C>T c.2332C>T (p.Leu778=) c.*28+8413C>T (n.*28+8413C>T) c.2197C>T (p.Leu733=) n.1230G>A c.1531C>T (p.Leu511=) | dbSNP gnomAD v4 |
7 | g.55181344_55181351del | CA891842019 | EGFR,EGFR-AS1 | c.2176_2183del (p.Gly726ProfsTer?) c.684_691del c.2335_2342del (p.Gly779ProfsTer?) c.*28+8416_*28+8423del (n.*28+8416_*28+8423del) c.2200_2207del (p.Gly734ProfsTer?) n.1223_1230del c.1534_1541del (p.Gly512ProfsTer?) | |
7 | g.55181342T>A | CA367578771 | EGFR,EGFR-AS1 | c.2174T>A (p.Leu725Gln) c.682T>A c.2333T>A (p.Leu778Gln) c.*28+8414T>A (n.*28+8414T>A) c.2198T>A (p.Leu733Gln) n.1229A>T c.1532T>A (p.Leu511Gln) | |
7 | g.55181342T>C | CA367578773 | EGFR,EGFR-AS1 | c.2174T>C (p.Leu725Pro) c.682T>C c.2333T>C (p.Leu778Pro) c.*28+8414T>C (n.*28+8414T>C) c.2198T>C (p.Leu733Pro) n.1229A>G c.1532T>C (p.Leu511Pro) | |
7 | g.55181342T>G | CA367578775 | EGFR,EGFR-AS1 | c.2174T>G (p.Leu725Arg) c.682T>G c.2333T>G (p.Leu778Arg) c.*28+8414T>G (n.*28+8414T>G) c.2198T>G (p.Leu733Arg) n.1229A>C c.1532T>G (p.Leu511Arg) | |
7 | g.55181343G>A | CA4266056 | EGFR,EGFR-AS1 | c.2175G>A (p.Leu725=) c.683G>A c.2334G>A (p.Leu778=) c.*28+8415G>A (n.*28+8415G>A) c.2199G>A (p.Leu733=) n.1228C>T c.1533G>A (p.Leu511=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.55181343G>C | CA455165109 | EGFR,EGFR-AS1 | c.2175G>C (p.Leu725=) c.683G>C c.2334G>C (p.Leu778=) c.*28+8415G>C (n.*28+8415G>C) c.2199G>C (p.Leu733=) n.1228C>G c.1533G>C (p.Leu511=) | dbSNP |
7 | g.55181343G= | CA1708905364 | EGFR,EGFR-AS1 | c.2175G= (p.Leu725=) c.683G= c.2334G= (p.Leu778=) c.*28+8415G= (n.*28+8415G=) c.2199G= (p.Leu733=) n.1228C= c.1533G= (p.Leu511=) | |
7 | g.55181343G>T | CA135878 | EGFR,EGFR-AS1 | c.2175G>T (p.Leu725=) c.683G>T c.2334G>T (p.Leu778=) c.*28+8415G>T (n.*28+8415G>T) c.2199G>T (p.Leu733=) n.1228C>A c.1533G>T (p.Leu511=) | ClinVar dbSNP COSMIC |
7 | g.55181345dup | CA2839978232 | EGFR,EGFR-AS1 | c.2177dup (p.Ile727HisfsTer?) c.685dup c.2336dup (p.Ile780HisfsTer?) c.*28+8417dup (n.*28+8417dup) c.2201dup (p.Ile735HisfsTer?) n.1228dup c.1535dup (p.Ile513HisfsTer?) | |
7 | g.55181344G>A | CA367578778 | EGFR,EGFR-AS1 | c.2176G>A (p.Gly726Ser) c.684G>A c.2335G>A (p.Gly779Ser) c.*28+8416G>A (n.*28+8416G>A) c.2200G>A (p.Gly734Ser) n.1227C>T c.1534G>A (p.Gly512Ser) | ClinVar dbSNP COSMIC |
7 | g.55181344G>C | CA367578781 | EGFR,EGFR-AS1 | c.2176G>C (p.Gly726Arg) c.684G>C c.2335G>C (p.Gly779Arg) c.*28+8416G>C (n.*28+8416G>C) c.2200G>C (p.Gly734Arg) n.1227C>G c.1534G>C (p.Gly512Arg) | dbSNP |
7 | g.55181344G= | CA1708905369 | EGFR,EGFR-AS1 | c.2176G= (p.Gly726=) c.684G= c.2335G= (p.Gly779=) c.*28+8416G= (n.*28+8416G=) c.2200G= (p.Gly734=) n.1227C= c.1534G= (p.Gly512=) | |
7 | g.55181344G>T | CA135881 | EGFR,EGFR-AS1 | c.2176G>T (p.Gly726Cys) c.684G>T c.2335G>T (p.Gly779Cys) c.*28+8416G>T (n.*28+8416G>T) c.2200G>T (p.Gly734Cys) n.1227C>A c.1534G>T (p.Gly512Cys) | ClinVar dbSNP gnomAD v3 gnomAD v4 COSMIC |
7 | g.55181344_55181345delinsTT | CA16040590 | EGFR,EGFR-AS1 | c.2176_2177delinsTT (p.Gly726Phe) c.684_685delinsTT c.2335_2336delinsTT (p.Gly779Phe) c.*28+8416_*28+8417delinsTT (n.*28+8416_*28+8417delinsTT) c.2200_2201delinsTT (p.Gly734Phe) n.1226_1227delinsAA c.1534_1535delinsTT (p.Gly512Phe) | COSMIC |
7 | g.55181345G>A | CA367578783 | EGFR,EGFR-AS1 | c.2177G>A (p.Gly726Asp) c.685G>A c.2336G>A (p.Gly779Asp) c.*28+8417G>A (n.*28+8417G>A) c.2201G>A (p.Gly734Asp) n.1226C>T c.1535G>A (p.Gly512Asp) | ClinVar dbSNP gnomAD v4 COSMIC |
7 | g.55181345G>C | CA367578784 | EGFR,EGFR-AS1 | c.2177G>C (p.Gly726Ala) c.685G>C c.2336G>C (p.Gly779Ala) c.*28+8417G>C (n.*28+8417G>C) c.2201G>C (p.Gly734Ala) n.1226C>G c.1535G>C (p.Gly512Ala) | dbSNP |
7 | g.55181345G= | CA1708905376 | EGFR,EGFR-AS1 | c.2177G= (p.Gly726=) c.685G= c.2336G= (p.Gly779=) c.*28+8417G= (n.*28+8417G=) c.2201G= (p.Gly734=) n.1226C= c.1535G= (p.Gly512=) | |
7 | g.55181345G>T | CA135884 | EGFR,EGFR-AS1 | c.2177G>T (p.Gly726Val) c.685G>T c.2336G>T (p.Gly779Val) c.*28+8417G>T (n.*28+8417G>T) c.2201G>T (p.Gly734Val) n.1226C>A c.1535G>T (p.Gly512Val) | ClinVar dbSNP |
7 | g.55181346C>A | CA455165113 | EGFR,EGFR-AS1 | c.2178C>A (p.Gly726=) c.686C>A c.2337C>A (p.Gly779=) c.*28+8418C>A (n.*28+8418C>A) c.2202C>A (p.Gly734=) n.1225G>T c.1536C>A (p.Gly512=) | dbSNP gnomAD v2 |
7 | g.55181346C= | CA1708905382 | EGFR,EGFR-AS1 | c.2178C= (p.Gly726=) c.686C= c.2337C= (p.Gly779=) c.*28+8418C= (n.*28+8418C=) c.2202C= (p.Gly734=) n.1225G= c.1536C= (p.Gly512=) | |
7 | g.55181346C>G | CA455165115 | EGFR,EGFR-AS1 | c.2178C>G (p.Gly726=) c.686C>G c.2337C>G (p.Gly779=) c.*28+8418C>G (n.*28+8418C>G) c.2202C>G (p.Gly734=) n.1225G>C c.1536C>G (p.Gly512=) | dbSNP |
7 | g.55181346C>T | CA455165116 | EGFR,EGFR-AS1 | c.2178C>T (p.Gly726=) c.686C>T c.2337C>T (p.Gly779=) c.*28+8418C>T (n.*28+8418C>T) c.2202C>T (p.Gly734=) n.1225G>A c.1536C>T (p.Gly512=) | dbSNP |
7 | g.55181347A>C | CA367578787 | EGFR,EGFR-AS1 | c.2179A>C (p.Ile727Leu) c.687A>C c.2338A>C (p.Ile780Leu) c.*28+8419A>C (n.*28+8419A>C) c.2203A>C (p.Ile735Leu) n.1224T>G c.1537A>C (p.Ile513Leu) | dbSNP |
7 | g.55181347A>G | CA367578785 | EGFR,EGFR-AS1 | c.2179A>G (p.Ile727Val) c.687A>G c.2338A>G (p.Ile780Val) c.*28+8419A>G (n.*28+8419A>G) c.2203A>G (p.Ile735Val) n.1224T>C c.1537A>G (p.Ile513Val) | dbSNP COSMIC |
7 | g.55181347A>T | CA367578786 | EGFR,EGFR-AS1 | c.2179A>T (p.Ile727Phe) c.687A>T c.2338A>T (p.Ile780Phe) c.*28+8419A>T (n.*28+8419A>T) c.2203A>T (p.Ile735Phe) n.1224T>A c.1537A>T (p.Ile513Phe) | dbSNP |
7 | g.55181348T>A | CA367578788 | EGFR,EGFR-AS1 | c.2180T>A (p.Ile727Asn) c.688T>A c.2339T>A (p.Ile780Asn) c.*28+8420T>A (n.*28+8420T>A) c.2204T>A (p.Ile735Asn) n.1223A>T c.1538T>A (p.Ile513Asn) | dbSNP |
7 | g.55181348T>C | CA367578790 | EGFR,EGFR-AS1 | c.2180T>C (p.Ile727Thr) c.688T>C c.2339T>C (p.Ile780Thr) c.*28+8420T>C (n.*28+8420T>C) c.2204T>C (p.Ile735Thr) n.1223A>G c.1538T>C (p.Ile513Thr) | ClinVar dbSNP COSMIC |
7 | g.55181348T>G | CA367578789 | EGFR,EGFR-AS1 | c.2180T>G (p.Ile727Ser) c.688T>G c.2339T>G (p.Ile780Ser) c.*28+8420T>G (n.*28+8420T>G) c.2204T>G (p.Ile735Ser) n.1223A>C c.1538T>G (p.Ile513Ser) | dbSNP COSMIC |
7 | g.55181348T= | CA1708905385 | EGFR,EGFR-AS1 | c.2180T= (p.Ile727=) c.688T= c.2339T= (p.Ile780=) c.*28+8420T= (n.*28+8420T=) c.2204T= (p.Ile735=) n.1223A= c.1538T= (p.Ile513=) | |
7 | g.55181349C>A | CA455165121 | EGFR,EGFR-AS1 | c.2181C>A (p.Ile727=) c.689C>A c.2340C>A (p.Ile780=) c.*28+8421C>A (n.*28+8421C>A) c.2205C>A (p.Ile735=) n.1222G>T c.1539C>A (p.Ile513=) | |
7 | g.55181349C= | CA1708905391 | EGFR,EGFR-AS1 | c.2181C= (p.Ile727=) c.689C= c.2340C= (p.Ile780=) c.*28+8421C= (n.*28+8421C=) c.2205C= (p.Ile735=) n.1222G= c.1539C= (p.Ile513=) | |
7 | g.55181349C>G | CA367578791 | EGFR,EGFR-AS1 | c.2181C>G (p.Ile727Met) c.689C>G c.2340C>G (p.Ile780Met) c.*28+8421C>G (n.*28+8421C>G) c.2205C>G (p.Ile735Met) n.1222G>C c.1539C>G (p.Ile513Met) | dbSNP |
7 | g.55181349C>T | CA135887 | EGFR,EGFR-AS1 | c.2181C>T (p.Ile727=) c.689C>T c.2340C>T (p.Ile780=) c.*28+8421C>T (n.*28+8421C>T) c.2205C>T (p.Ile735=) n.1222G>A c.1539C>T (p.Ile513=) | ClinVar dbSNP |
7 | g.55181350T>A | CA367578792 | EGFR,EGFR-AS1 | c.2182T>A (p.Cys728Ser) c.690T>A c.2341T>A (p.Cys781Ser) c.*28+8422T>A (n.*28+8422T>A) c.2206T>A (p.Cys736Ser) n.1221A>T c.1540T>A (p.Cys514Ser) | dbSNP |
7 | g.55181350T>C | CA367578793 | EGFR,EGFR-AS1 | c.2182T>C (p.Cys728Arg) c.690T>C c.2341T>C (p.Cys781Arg) c.*28+8422T>C (n.*28+8422T>C) c.2206T>C (p.Cys736Arg) n.1221A>G c.1540T>C (p.Cys514Arg) | dbSNP |
7 | g.55181350T>G | CA367578794 | EGFR,EGFR-AS1 | c.2182T>G (p.Cys728Gly) c.690T>G c.2341T>G (p.Cys781Gly) c.*28+8422T>G (n.*28+8422T>G) c.2206T>G (p.Cys736Gly) n.1221A>C c.1540T>G (p.Cys514Gly) | |
7 | g.55181351G>A | CA367578795 | EGFR,EGFR-AS1 | c.2183G>A (p.Cys728Tyr) c.691G>A c.2342G>A (p.Cys781Tyr) c.*28+8423G>A (n.*28+8423G>A) c.2207G>A (p.Cys736Tyr) n.1220C>T c.1541G>A (p.Cys514Tyr) | dbSNP gnomAD v4 |
7 | g.55181351G>C | CA367578796 | EGFR,EGFR-AS1 | c.2183G>C (p.Cys728Ser) c.691G>C c.2342G>C (p.Cys781Ser) c.*28+8423G>C (n.*28+8423G>C) c.2207G>C (p.Cys736Ser) n.1220C>G c.1541G>C (p.Cys514Ser) | dbSNP |
7 | g.55181351G>T | CA367578797 | EGFR,EGFR-AS1 | c.2183G>T (p.Cys728Phe) c.691G>T c.2342G>T (p.Cys781Phe) c.*28+8423G>T (n.*28+8423G>T) c.2207G>T (p.Cys736Phe) n.1220C>A c.1541G>T (p.Cys514Phe) | COSMIC |
7 | g.55181352C>A | CA367578798 | EGFR,EGFR-AS1 | c.2184C>A (p.Cys728Ter) c.692C>A c.2343C>A (p.Cys781Ter) c.*28+8424C>A (n.*28+8424C>A) c.2208C>A (p.Cys736Ter) n.1219G>T c.1542C>A (p.Cys514Ter) | dbSNP |
7 | g.55181352C>G | CA367578799 | EGFR,EGFR-AS1 | c.2184C>G (p.Cys728Trp) c.692C>G c.2343C>G (p.Cys781Trp) c.*28+8424C>G (n.*28+8424C>G) c.2208C>G (p.Cys736Trp) n.1219G>C c.1542C>G (p.Cys514Trp) | dbSNP |
7 | g.55181352C>T | CA455165127 | EGFR,EGFR-AS1 | c.2184C>T (p.Cys728=) c.692C>T c.2343C>T (p.Cys781=) c.*28+8424C>T (n.*28+8424C>T) c.2208C>T (p.Cys736=) n.1219G>A c.1542C>T (p.Cys514=) | dbSNP |
7 | g.55181353C>A | CA367578800 | EGFR,EGFR-AS1 | c.2185C>A (p.Leu729Ile) c.693C>A c.2344C>A (p.Leu782Ile) c.*28+8425C>A (n.*28+8425C>A) c.2209C>A (p.Leu737Ile) n.1218G>T c.1543C>A (p.Leu515Ile) | dbSNP |
7 | g.55181353C>G | CA367578801 | EGFR,EGFR-AS1 | c.2185C>G (p.Leu729Val) c.693C>G c.2344C>G (p.Leu782Val) c.*28+8425C>G (n.*28+8425C>G) c.2209C>G (p.Leu737Val) n.1218G>C c.1543C>G (p.Leu515Val) | |
7 | g.55181353C>T | CA367578802 | EGFR,EGFR-AS1 | c.2185C>T (p.Leu729Phe) c.693C>T c.2344C>T (p.Leu782Phe) c.*28+8425C>T (n.*28+8425C>T) c.2209C>T (p.Leu737Phe) n.1218G>A c.1543C>T (p.Leu515Phe) | dbSNP |
7 | g.55181353_55181354delinsAA | CA645561608 | EGFR,EGFR-AS1 | c.2185_2186delinsAA (p.Leu729Asn) c.693_694delinsAA c.2344_2345delinsAA (p.Leu782Asn) c.*28+8425_*28+8426delinsAA (n.*28+8425_*28+8426delinsAA) c.2209_2210delinsAA (p.Leu737Asn) n.1217_1218delinsTT c.1543_1544delinsAA (p.Leu515Asn) | COSMIC |
7 | g.55181354T>A | CA367578805 | EGFR,EGFR-AS1 | c.2186T>A (p.Leu729His) c.694T>A c.2345T>A (p.Leu782His) c.*28+8426T>A (n.*28+8426T>A) c.2210T>A (p.Leu737His) n.1217A>T c.1544T>A (p.Leu515His) | |
7 | g.55181354T>C | CA367578803 | EGFR,EGFR-AS1 | c.2186T>C (p.Leu729Pro) c.694T>C c.2345T>C (p.Leu782Pro) c.*28+8426T>C (n.*28+8426T>C) c.2210T>C (p.Leu737Pro) n.1217A>G c.1544T>C (p.Leu515Pro) | |
7 | g.55181354T>G | CA367578804 | EGFR,EGFR-AS1 | c.2186T>G (p.Leu729Arg) c.694T>G c.2345T>G (p.Leu782Arg) c.*28+8426T>G (n.*28+8426T>G) c.2210T>G (p.Leu737Arg) n.1217A>C c.1544T>G (p.Leu515Arg) | |
7 | g.55181355C>A | CA455165130 | EGFR,EGFR-AS1 | c.2187C>A (p.Leu729=) c.695C>A c.2346C>A (p.Leu782=) c.*28+8427C>A (n.*28+8427C>A) c.2211C>A (p.Leu737=) n.1216G>T c.1545C>A (p.Leu515=) | dbSNP gnomAD v3 gnomAD v4 |
7 | g.55181355C= | CA1708905395 | EGFR,EGFR-AS1 | c.2187C= (p.Leu729=) c.695C= c.2346C= (p.Leu782=) c.*28+8427C= (n.*28+8427C=) c.2211C= (p.Leu737=) n.1216G= c.1545C= (p.Leu515=) | |
7 | g.55181355C>G | CA455165132 | EGFR,EGFR-AS1 | c.2187C>G (p.Leu729=) c.695C>G c.2346C>G (p.Leu782=) c.*28+8427C>G (n.*28+8427C>G) c.2211C>G (p.Leu737=) n.1216G>C c.1545C>G (p.Leu515=) | dbSNP gnomAD v4 |
7 | g.55181355C>T | CA455165133 | EGFR,EGFR-AS1 | c.2187C>T (p.Leu729=) c.695C>T c.2346C>T (p.Leu782=) c.*28+8427C>T (n.*28+8427C>T) c.2211C>T (p.Leu737=) n.1216G>A c.1545C>T (p.Leu515=) | ClinVar dbSNP gnomAD v4 |
7 | g.55181356A>C | CA367578806 | EGFR,EGFR-AS1 | c.2188A>C (p.Thr730Pro) c.696A>C c.2347A>C (p.Thr783Pro) c.*28+8428A>C (n.*28+8428A>C) c.2212A>C (p.Thr738Pro) n.1215T>G c.1546A>C (p.Thr516Pro) | dbSNP |
7 | g.55181356A>G | CA367578807 | EGFR,EGFR-AS1 | c.2188A>G (p.Thr730Ala) c.696A>G c.2347A>G (p.Thr783Ala) c.*28+8428A>G (n.*28+8428A>G) c.2212A>G (p.Thr738Ala) n.1215T>C c.1546A>G (p.Thr516Ala) | dbSNP |
7 | g.55181356A>T | CA367578808 | EGFR,EGFR-AS1 | c.2188A>T (p.Thr730Ser) c.696A>T c.2347A>T (p.Thr783Ser) c.*28+8428A>T (n.*28+8428A>T) c.2212A>T (p.Thr738Ser) n.1215T>A c.1546A>T (p.Thr516Ser) | dbSNP |
7 | g.55181357C>A | CA367578809 | EGFR,EGFR-AS1 | c.2189C>A (p.Thr730Asn) c.697C>A c.2348C>A (p.Thr783Asn) c.*28+8429C>A (n.*28+8429C>A) c.2213C>A (p.Thr738Asn) n.1214G>T c.1547C>A (p.Thr516Asn) | dbSNP |
7 | g.55181357C>G | CA367578810 | EGFR,EGFR-AS1 | c.2189C>G (p.Thr730Ser) c.697C>G c.2348C>G (p.Thr783Ser) c.*28+8429C>G (n.*28+8429C>G) c.2213C>G (p.Thr738Ser) n.1214G>C c.1547C>G (p.Thr516Ser) | dbSNP |
7 | g.55181357C>T | CA367578811 | EGFR,EGFR-AS1 | c.2189C>T (p.Thr730Ile) c.697C>T c.2348C>T (p.Thr783Ile) c.*28+8429C>T (n.*28+8429C>T) c.2213C>T (p.Thr738Ile) n.1214G>A c.1547C>T (p.Thr516Ile) | dbSNP COSMIC |
7 | g.55181358C>A | CA4266057 | EGFR,EGFR-AS1 | c.2190C>A (p.Thr730=) c.698C>A c.2349C>A (p.Thr783=) c.*28+8430C>A (n.*28+8430C>A) c.2214C>A (p.Thr738=) n.1213G>T c.1548C>A (p.Thr516=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
7 | g.55181358C= | CA1708905403 | EGFR,EGFR-AS1 | c.2190C= (p.Thr730=) c.698C= c.2349C= (p.Thr783=) c.*28+8430C= (n.*28+8430C=) c.2214C= (p.Thr738=) n.1213G= c.1548C= (p.Thr516=) | |
7 | g.55181358C>G | CA455165137 | EGFR,EGFR-AS1 | c.2190C>G (p.Thr730=) c.698C>G c.2349C>G (p.Thr783=) c.*28+8430C>G (n.*28+8430C>G) c.2214C>G (p.Thr738=) n.1213G>C c.1548C>G (p.Thr516=) | dbSNP |
7 | g.55181358C>T | CA135890 | EGFR,EGFR-AS1 | c.2190C>T (p.Thr730=) c.698C>T c.2349C>T (p.Thr783=) c.*28+8430C>T (n.*28+8430C>T) c.2214C>T (p.Thr738=) n.1213G>A c.1548C>T (p.Thr516=) | ClinVar dbSNP gnomAD v4 |
7 | g.55181359T>A | CA367578812 | EGFR,EGFR-AS1 | c.2191T>A (p.Ser731Thr) c.699T>A c.2350T>A (p.Ser784Thr) c.*28+8431T>A (n.*28+8431T>A) c.2215T>A (p.Ser739Thr) n.1212A>T c.1549T>A (p.Ser517Thr) | |
7 | g.55181359T>C | CA367578813 | EGFR,EGFR-AS1 | c.2191T>C (p.Ser731Pro) c.699T>C c.2350T>C (p.Ser784Pro) c.*28+8431T>C (n.*28+8431T>C) c.2215T>C (p.Ser739Pro) n.1212A>G c.1549T>C (p.Ser517Pro) | dbSNP gnomAD v4 COSMIC |
7 | g.55181359T>G | CA367578814 | EGFR,EGFR-AS1 | c.2191T>G (p.Ser731Ala) c.699T>G c.2350T>G (p.Ser784Ala) c.*28+8431T>G (n.*28+8431T>G) c.2215T>G (p.Ser739Ala) n.1212A>C c.1549T>G (p.Ser517Ala) | |
7 | g.55181360C>A | CA367578816 | EGFR,EGFR-AS1 | c.2192C>A (p.Ser731Tyr) c.700C>A c.2351C>A (p.Ser784Tyr) c.*28+8432C>A (n.*28+8432C>A) c.2216C>A (p.Ser739Tyr) n.1211G>T c.1550C>A (p.Ser517Tyr) | dbSNP COSMIC |
7 | g.55181360C= | CA1708905409 | EGFR,EGFR-AS1 | c.2192C= (p.Ser731=) c.700C= c.2351C= (p.Ser784=) c.*28+8432C= (n.*28+8432C=) c.2216C= (p.Ser739=) n.1211G= c.1550C= (p.Ser517=) | |
7 | g.55181360C>G | CA367578817 | EGFR,EGFR-AS1 | c.2192C>G (p.Ser731Cys) c.700C>G c.2351C>G (p.Ser784Cys) c.*28+8432C>G (n.*28+8432C>G) c.2216C>G (p.Ser739Cys) n.1211G>C c.1550C>G (p.Ser517Cys) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.55181360C>T | CA367578815 | EGFR,EGFR-AS1 | c.2192C>T (p.Ser731Phe) c.700C>T c.2351C>T (p.Ser784Phe) c.*28+8432C>T (n.*28+8432C>T) c.2216C>T (p.Ser739Phe) n.1211G>A c.1550C>T (p.Ser517Phe) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
7 | g.55181361C>A | CA455165144 | EGFR,EGFR-AS1 | c.2193C>A (p.Ser731=) c.701C>A c.2352C>A (p.Ser784=) c.*28+8433C>A (n.*28+8433C>A) c.2217C>A (p.Ser739=) n.1210G>T c.1551C>A (p.Ser517=) | |
7 | g.55181361C>G | CA455165145 | EGFR,EGFR-AS1 | c.2193C>G (p.Ser731=) c.701C>G c.2352C>G (p.Ser784=) c.*28+8433C>G (n.*28+8433C>G) c.2217C>G (p.Ser739=) n.1210G>C c.1551C>G (p.Ser517=) | dbSNP |
7 | g.55181361C>T | CA455165146 | EGFR,EGFR-AS1 | c.2193C>T (p.Ser731=) c.701C>T c.2352C>T (p.Ser784=) c.*28+8433C>T (n.*28+8433C>T) c.2217C>T (p.Ser739=) n.1210G>A c.1551C>T (p.Ser517=) | ClinVar dbSNP |
7 | g.55181362A>C | CA367578818 | EGFR,EGFR-AS1 | c.2194A>C (p.Thr732Pro) c.702A>C c.2353A>C (p.Thr785Pro) c.*28+8434A>C (n.*28+8434A>C) c.2218A>C (p.Thr740Pro) n.1209T>G c.1552A>C (p.Thr518Pro) | dbSNP COSMIC |
7 | g.55181362A>G | CA367578819 | EGFR,EGFR-AS1 | c.2194A>G (p.Thr732Ala) c.702A>G c.2353A>G (p.Thr785Ala) c.*28+8434A>G (n.*28+8434A>G) c.2218A>G (p.Thr740Ala) n.1209T>C c.1552A>G (p.Thr518Ala) | ClinVar dbSNP gnomAD v4 COSMIC |
7 | g.55181362A>T | CA367578820 | EGFR,EGFR-AS1 | c.2194A>T (p.Thr732Ser) c.702A>T c.2353A>T (p.Thr785Ser) c.*28+8434A>T (n.*28+8434A>T) c.2218A>T (p.Thr740Ser) n.1209T>A c.1552A>T (p.Thr518Ser) | |
7 | g.55181363C>A | CA367578821 | EGFR,EGFR-AS1 | c.2195C>A (p.Thr732Asn) c.703C>A c.2354C>A (p.Thr785Asn) c.*28+8435C>A (n.*28+8435C>A) c.2219C>A (p.Thr740Asn) n.1208G>T c.1553C>A (p.Thr518Asn) | dbSNP COSMIC |
7 | g.55181363C>G | CA367578822 | EGFR,EGFR-AS1 | c.2195C>G (p.Thr732Ser) c.703C>G c.2354C>G (p.Thr785Ser) c.*28+8435C>G (n.*28+8435C>G) c.2219C>G (p.Thr740Ser) n.1208G>C c.1553C>G (p.Thr518Ser) | dbSNP |
7 | g.55181363C>T | CA367578823 | EGFR,EGFR-AS1 | c.2195C>T (p.Thr732Ile) c.703C>T c.2354C>T (p.Thr785Ile) c.*28+8435C>T (n.*28+8435C>T) c.2219C>T (p.Thr740Ile) n.1208G>A c.1553C>T (p.Thr518Ile) | dbSNP COSMIC |
7 | g.55181364C>A | CA455165150 | EGFR,EGFR-AS1 | c.2196C>A (p.Thr732=) c.704C>A c.2355C>A (p.Thr785=) c.*28+8436C>A (n.*28+8436C>A) c.2220C>A (p.Thr740=) n.1207G>T c.1554C>A (p.Thr518=) | dbSNP gnomAD v2 gnomAD v4 |
7 | g.55181364C= | CA1708905414 | EGFR,EGFR-AS1 | c.2196C= (p.Thr732=) c.704C= c.2355C= (p.Thr785=) c.*28+8436C= (n.*28+8436C=) c.2220C= (p.Thr740=) n.1207G= c.1554C= (p.Thr518=) | |
7 | g.55181364C>G | CA455165151 | EGFR,EGFR-AS1 | c.2196C>G (p.Thr732=) c.704C>G c.2355C>G (p.Thr785=) c.*28+8436C>G (n.*28+8436C>G) c.2220C>G (p.Thr740=) n.1207G>C c.1554C>G (p.Thr518=) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
7 | g.55181364C>T | CA135893 | EGFR,EGFR-AS1 | c.2196C>T (p.Thr732=) c.704C>T c.2355C>T (p.Thr785=) c.*28+8436C>T (n.*28+8436C>T) c.2220C>T (p.Thr740=) n.1207G>A c.1554C>T (p.Thr518=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.55181365G>A | CA4266058 | EGFR,EGFR-AS1 | c.2197G>A (p.Val733Met) c.705G>A c.2356G>A (p.Val786Met) c.*28+8437G>A (n.*28+8437G>A) c.2221G>A (p.Val741Met) n.1206C>T c.1555G>A (p.Val519Met) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
7 | g.55181365G>C | CA367578825 | EGFR,EGFR-AS1 | c.2197G>C (p.Val733Leu) c.705G>C c.2356G>C (p.Val786Leu) c.*28+8437G>C (n.*28+8437G>C) c.2221G>C (p.Val741Leu) n.1206C>G c.1555G>C (p.Val519Leu) | dbSNP gnomAD v2 |
7 | g.55181365G= | CA1708905428 | EGFR,EGFR-AS1 | c.2197G= (p.Val733=) c.705G= c.2356G= (p.Val786=) c.*28+8437G= (n.*28+8437G=) c.2221G= (p.Val741=) n.1206C= c.1555G= (p.Val519=) | |
7 | g.55181365G>T | CA367578824 | EGFR,EGFR-AS1 | c.2197G>T (p.Val733Leu) c.705G>T c.2356G>T (p.Val786Leu) c.*28+8437G>T (n.*28+8437G>T) c.2221G>T (p.Val741Leu) n.1206C>A c.1555G>T (p.Val519Leu) | |
7 | g.55181366T>A | CA367578826 | EGFR,EGFR-AS1 | c.2198T>A (p.Val733Glu) c.706T>A c.2357T>A (p.Val786Glu) c.*28+8438T>A (n.*28+8438T>A) c.2222T>A (p.Val741Glu) n.1205A>T c.1556T>A (p.Val519Glu) | ClinVar dbSNP gnomAD v4 |
7 | g.55181366T>C | CA367578827 | EGFR,EGFR-AS1 | c.2198T>C (p.Val733Ala) c.706T>C c.2357T>C (p.Val786Ala) c.*28+8438T>C (n.*28+8438T>C) c.2222T>C (p.Val741Ala) n.1205A>G c.1556T>C (p.Val519Ala) | gnomAD v4 |
7 | g.55181366T>G | CA367578828 | EGFR,EGFR-AS1 | c.2198T>G (p.Val733Gly) c.706T>G c.2357T>G (p.Val786Gly) c.*28+8438T>G (n.*28+8438T>G) c.2222T>G (p.Val741Gly) n.1205A>C c.1556T>G (p.Val519Gly) | |
7 | g.55181367G>A | CA4266059 | EGFR,EGFR-AS1 | c.2199G>A (p.Val733=) c.707G>A c.2358G>A (p.Val786=) c.*28+8439G>A (n.*28+8439G>A) c.2223G>A (p.Val741=) n.1204C>T c.1557G>A (p.Val519=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
7 | g.55181367G>C | CA455165155 | EGFR,EGFR-AS1 | c.2199G>C (p.Val733=) c.707G>C c.2358G>C (p.Val786=) c.*28+8439G>C (n.*28+8439G>C) c.2223G>C (p.Val741=) n.1204C>G c.1557G>C (p.Val519=) | dbSNP gnomAD v4 |
7 | g.55181367G= | CA1708905439 | EGFR,EGFR-AS1 | c.2199G= (p.Val733=) c.707G= c.2358G= (p.Val786=) c.*28+8439G= (n.*28+8439G=) c.2223G= (p.Val741=) n.1204C= c.1557G= (p.Val519=) | |
7 | g.55181367G>T | CA455165156 | EGFR,EGFR-AS1 | c.2199G>T (p.Val733=) c.707G>T c.2358G>T (p.Val786=) c.*28+8439G>T (n.*28+8439G>T) c.2223G>T (p.Val741=) n.1204C>A c.1557G>T (p.Val519=) | dbSNP |
7 | g.55181376_55181387dup | CA2697557280 | EGFR,EGFR-AS1 | c.2208_2219dup (p.Leu739_Met740insIleThrGlnLeu) c.716_727dup c.2367_2378dup (p.Leu792_Met793insIleThrGlnLeu) c.*28+8448_*28+8459dup (n.*28+8448_*28+8459dup) c.2232_2243dup (p.Leu747_Met748insIleThrGlnLeu) n.1193_1204dup c.1566_1577dup (p.Leu525_Met526insIleThrGlnLeu) | ClinVar |
7 | g.55181368C>A | CA367578829 | EGFR,EGFR-AS1 | c.2200C>A (p.Gln734Lys) c.708C>A c.2359C>A (p.Gln787Lys) c.*28+8440C>A (n.*28+8440C>A) c.2224C>A (p.Gln742Lys) n.1203G>T c.1558C>A (p.Gln520Lys) | |
7 | g.55181368C>G | CA367578831 | EGFR,EGFR-AS1 | c.2200C>G (p.Gln734Glu) c.708C>G c.2359C>G (p.Gln787Glu) c.*28+8440C>G (n.*28+8440C>G) c.2224C>G (p.Gln742Glu) n.1203G>C c.1558C>G (p.Gln520Glu) | |
7 | g.55181368C>T | CA367578830 | EGFR,EGFR-AS1 | c.2200C>T (p.Gln734Ter) c.708C>T c.2359C>T (p.Gln787Ter) c.*28+8440C>T (n.*28+8440C>T) c.2224C>T (p.Gln742Ter) n.1203G>A c.1558C>T (p.Gln520Ter) | |
7 | g.55181369A= | CA1708905448 | EGFR,EGFR-AS1 | c.2201A= (p.Gln734=) c.709A= c.2360A= (p.Gln787=) c.*28+8441A= (n.*28+8441A=) c.2225A= (p.Gln742=) n.1202T= c.1559A= (p.Gln520=) | |
7 | g.55181369A>C | CA367578832 | EGFR,EGFR-AS1 | c.2201A>C (p.Gln734Pro) c.709A>C c.2360A>C (p.Gln787Pro) c.*28+8441A>C (n.*28+8441A>C) c.2225A>C (p.Gln742Pro) n.1202T>G c.1559A>C (p.Gln520Pro) | dbSNP gnomAD v2 |
7 | g.55181369A>G | CA367578833 | EGFR,EGFR-AS1 | c.2201A>G (p.Gln734Arg) c.709A>G c.2360A>G (p.Gln787Arg) c.*28+8441A>G (n.*28+8441A>G) c.2225A>G (p.Gln742Arg) n.1202T>C c.1559A>G (p.Gln520Arg) | COSMIC |
7 | g.55181369A>T | CA367578834 | EGFR,EGFR-AS1 | c.2201A>T (p.Gln734Leu) c.709A>T c.2360A>T (p.Gln787Leu) c.*28+8441A>T (n.*28+8441A>T) c.2225A>T (p.Gln742Leu) n.1202T>A c.1559A>T (p.Gln520Leu) | |
7 | g.55181369dup | CA2841308928 | EGFR,EGFR-AS1 | c.2201dup (p.Leu735AlafsTer?) c.709dup c.2360dup (p.Leu788AlafsTer?) c.*28+8441dup (n.*28+8441dup) c.2225dup (p.Leu743AlafsTer?) n.1202dup c.1559dup (p.Leu521AlafsTer?) | |
7 | g.55181370G>A | CA135896 | EGFR,EGFR-AS1 | c.2202G>A (p.Gln734=) c.710G>A c.2361G>A (p.Gln787=) c.*28+8442G>A (n.*28+8442G>A) c.2226G>A (p.Gln742=) n.1201C>T c.1560G>A (p.Gln520=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.55181370G>C | CA367578835 | EGFR,EGFR-AS1 | c.2202G>C (p.Gln734His) c.710G>C c.2361G>C (p.Gln787His) c.*28+8442G>C (n.*28+8442G>C) c.2226G>C (p.Gln742His) n.1201C>G c.1560G>C (p.Gln520His) | dbSNP |
7 | g.55181370G= | CA1708905453 | EGFR,EGFR-AS1 | c.2202G= (p.Gln734=) c.710G= c.2361G= (p.Gln787=) c.*28+8442G= (n.*28+8442G=) c.2226G= (p.Gln742=) n.1201C= c.1560G= (p.Gln520=) | |
7 | g.55181370G>T | CA367578836 | EGFR,EGFR-AS1 | c.2202G>T (p.Gln734His) c.710G>T c.2361G>T (p.Gln787His) c.*28+8442G>T (n.*28+8442G>T) c.2226G>T (p.Gln742His) n.1201C>A c.1560G>T (p.Gln520His) | ClinVar dbSNP |
7 | g.55181370_55181371delinsAA | CA2573142238 | EGFR,EGFR-AS1 | c.2202_2203delinsAA (p.Leu735Ile) c.710_711delinsAA c.2361_2362delinsAA (p.Leu788Ile) c.*28+8442_*28+8443delinsAA (n.*28+8442_*28+8443delinsAA) c.2226_2227delinsAA (p.Leu743Ile) n.1200_1201delinsTT c.1560_1561delinsAA (p.Leu521Ile) | ClinVar dbSNP |
7 | g.55181370_55181371insTGCAA | CA918009551 | EGFR,EGFR-AS1 | c.2202_2203insTGCAA (p.Leu735CysfsTer?) c.710_711insTGCAA c.2361_2362insTGCAA (p.Leu788CysfsTer?) c.*28+8442_*28+8443insTGCAA (n.*28+8442_*28+8443insTGCAA) c.2226_2227insTGCAA (p.Leu743CysfsTer?) n.1200_1201insTTGCA c.1560_1561insTGCAA (p.Leu521CysfsTer?) | dbSNP gnomAD v4 |
7 | g.55181371C>A | CA367578837 | EGFR,EGFR-AS1 | c.2203C>A (p.Leu735Ile) c.711C>A c.2362C>A (p.Leu788Ile) c.*28+8443C>A (n.*28+8443C>A) c.2227C>A (p.Leu743Ile) n.1200G>T c.1561C>A (p.Leu521Ile) | dbSNP |
7 | g.55181371C>G | CA367578838 | EGFR,EGFR-AS1 | c.2203C>G (p.Leu735Val) c.711C>G c.2362C>G (p.Leu788Val) c.*28+8443C>G (n.*28+8443C>G) c.2227C>G (p.Leu743Val) n.1200G>C c.1561C>G (p.Leu521Val) | dbSNP |
7 | g.55181371C>T | CA367578839 | EGFR,EGFR-AS1 | c.2203C>T (p.Leu735Phe) c.711C>T c.2362C>T (p.Leu788Phe) c.*28+8443C>T (n.*28+8443C>T) c.2227C>T (p.Leu743Phe) n.1200G>A c.1561C>T (p.Leu521Phe) | dbSNP gnomAD v4 |
7 | g.55181372T>A | CA367578840 | EGFR,EGFR-AS1 | c.2204T>A (p.Leu735His) c.712T>A c.2363T>A (p.Leu788His) c.*28+8444T>A (n.*28+8444T>A) c.2228T>A (p.Leu743His) n.1199A>T c.1562T>A (p.Leu521His) | dbSNP |
7 | g.55181372T>C | CA367578841 | EGFR,EGFR-AS1 | c.2204T>C (p.Leu735Pro) c.712T>C c.2363T>C (p.Leu788Pro) c.*28+8444T>C (n.*28+8444T>C) c.2228T>C (p.Leu743Pro) n.1199A>G c.1562T>C (p.Leu521Pro) | dbSNP |
7 | g.55181372T>G | CA367578842 | EGFR,EGFR-AS1 | c.2204T>G (p.Leu735Arg) c.712T>G c.2363T>G (p.Leu788Arg) c.*28+8444T>G (n.*28+8444T>G) c.2228T>G (p.Leu743Arg) n.1199A>C c.1562T>G (p.Leu521Arg) | |
7 | g.55181373C>A | CA455165161 | EGFR,EGFR-AS1 | c.2205C>A (p.Leu735=) c.713C>A c.2364C>A (p.Leu788=) c.*28+8445C>A (n.*28+8445C>A) c.2229C>A (p.Leu743=) n.1198G>T c.1563C>A (p.Leu521=) | dbSNP |
7 | g.55181373C= | CA1708905465 | EGFR,EGFR-AS1 | c.2205C= (p.Leu735=) c.713C= c.2364C= (p.Leu788=) c.*28+8445C= (n.*28+8445C=) c.2229C= (p.Leu743=) n.1198G= c.1563C= (p.Leu521=) | |
7 | g.55181373C>G | CA455165162 | EGFR,EGFR-AS1 | c.2205C>G (p.Leu735=) c.713C>G c.2364C>G (p.Leu788=) c.*28+8445C>G (n.*28+8445C>G) c.2229C>G (p.Leu743=) n.1198G>C c.1563C>G (p.Leu521=) | dbSNP |
7 | g.55181373C>T | CA4266060 | EGFR,EGFR-AS1 | c.2205C>T (p.Leu735=) c.713C>T c.2364C>T (p.Leu788=) c.*28+8445C>T (n.*28+8445C>T) c.2229C>T (p.Leu743=) n.1198G>A c.1563C>T (p.Leu521=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.55181374A= | CA1708905470 | EGFR,EGFR-AS1 | c.2206A= (p.Ile736=) c.714A= c.2365A= (p.Ile789=) c.*28+8446A= (n.*28+8446A=) c.2230A= (p.Ile744=) n.1197T= c.1564A= (p.Ile522=) | |
7 | g.55181374A>C | CA4266061 | EGFR,EGFR-AS1 | c.2206A>C (p.Ile736Leu) c.714A>C c.2365A>C (p.Ile789Leu) c.*28+8446A>C (n.*28+8446A>C) c.2230A>C (p.Ile744Leu) n.1197T>G c.1564A>C (p.Ile522Leu) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
7 | g.55181374A>G | CA367578843 | EGFR,EGFR-AS1 | c.2206A>G (p.Ile736Val) c.714A>G c.2365A>G (p.Ile789Val) c.*28+8446A>G (n.*28+8446A>G) c.2230A>G (p.Ile744Val) n.1197T>C c.1564A>G (p.Ile522Val) | ClinVar |
7 | g.55181374A>T | CA367578844 | EGFR,EGFR-AS1 | c.2206A>T (p.Ile736Phe) c.714A>T c.2365A>T (p.Ile789Phe) c.*28+8446A>T (n.*28+8446A>T) c.2230A>T (p.Ile744Phe) n.1197T>A c.1564A>T (p.Ile522Phe) | dbSNP |
7 | g.55181375T>A | CA367578845 | EGFR,EGFR-AS1 | c.2207T>A (p.Ile736Asn) c.715T>A c.2366T>A (p.Ile789Asn) c.*28+8447T>A (n.*28+8447T>A) c.2231T>A (p.Ile744Asn) n.1196A>T c.1565T>A (p.Ile522Asn) | dbSNP |
7 | g.55181375T>C | CA367578846 | EGFR,EGFR-AS1 | c.2207T>C (p.Ile736Thr) c.715T>C c.2366T>C (p.Ile789Thr) c.*28+8447T>C (n.*28+8447T>C) c.2231T>C (p.Ile744Thr) n.1196A>G c.1565T>C (p.Ile522Thr) | gnomAD v4 |
7 | g.55181375T>G | CA367578847 | EGFR,EGFR-AS1 | c.2207T>G (p.Ile736Ser) c.715T>G c.2366T>G (p.Ile789Ser) c.*28+8447T>G (n.*28+8447T>G) c.2231T>G (p.Ile744Ser) n.1196A>C c.1565T>G (p.Ile522Ser) | dbSNP |
7 | g.55181376C>A | CA455165165 | EGFR,EGFR-AS1 | c.2208C>A (p.Ile736=) c.716C>A c.2367C>A (p.Ile789=) c.*28+8448C>A (n.*28+8448C>A) c.2232C>A (p.Ile744=) n.1195G>T c.1566C>A (p.Ile522=) | dbSNP |
7 | g.55181376C= | CA1708905477 | EGFR,EGFR-AS1 | c.2208C= (p.Ile736=) c.716C= c.2367C= (p.Ile789=) c.*28+8448C= (n.*28+8448C=) c.2232C= (p.Ile744=) n.1195G= c.1566C= (p.Ile522=) | |
7 | g.55181376C>G | CA367578848 | EGFR,EGFR-AS1 | c.2208C>G (p.Ile736Met) c.716C>G c.2367C>G (p.Ile789Met) c.*28+8448C>G (n.*28+8448C>G) c.2232C>G (p.Ile744Met) n.1195G>C c.1566C>G (p.Ile522Met) | dbSNP COSMIC |
7 | g.55181376C>T | CA455165166 | EGFR,EGFR-AS1 | c.2208C>T (p.Ile736=) c.716C>T c.2367C>T (p.Ile789=) c.*28+8448C>T (n.*28+8448C>T) c.2232C>T (p.Ile744=) n.1195G>A c.1566C>T (p.Ile522=) | ClinVar dbSNP |
7 | g.55181377A>C | CA367578849 | EGFR,EGFR-AS1 | c.2209A>C (p.Thr737Pro) c.717A>C c.2368A>C (p.Thr790Pro) c.*28+8449A>C (n.*28+8449A>C) c.2233A>C (p.Thr745Pro) n.1194T>G c.1567A>C (p.Thr523Pro) | dbSNP |
7 | g.55181377A>G | CA367578850 | EGFR,EGFR-AS1 | c.2209A>G (p.Thr737Ala) c.717A>G c.2368A>G (p.Thr790Ala) c.*28+8449A>G (n.*28+8449A>G) c.2233A>G (p.Thr745Ala) n.1194T>C c.1567A>G (p.Thr523Ala) | dbSNP COSMIC |
7 | g.55181377A>T | CA367578851 | EGFR,EGFR-AS1 | c.2209A>T (p.Thr737Ser) c.717A>T c.2368A>T (p.Thr790Ser) c.*28+8449A>T (n.*28+8449A>T) c.2233A>T (p.Thr745Ser) n.1194T>A c.1567A>T (p.Thr523Ser) | ClinVar dbSNP |
7 | g.55181378C>A | CA367578852 | EGFR,EGFR-AS1 | c.2210C>A (p.Thr737Lys) c.718C>A c.2369C>A (p.Thr790Lys) c.*28+8450C>A (n.*28+8450C>A) c.2234C>A (p.Thr745Lys) n.1193G>T c.1568C>A (p.Thr523Lys) | gnomAD v4 |
7 | g.55181378C= | CA1708905489 | EGFR,EGFR-AS1 | c.2210C= (p.Thr737=) c.718C= c.2369C= (p.Thr790=) c.*28+8450C= (n.*28+8450C=) c.2234C= (p.Thr745=) n.1193G= c.1568C= (p.Thr523=) | |
7 | g.55181378C>G | CA367578853 | EGFR,EGFR-AS1 | c.2210C>G (p.Thr737Arg) c.718C>G c.2369C>G (p.Thr790Arg) c.*28+8450C>G (n.*28+8450C>G) c.2234C>G (p.Thr745Arg) n.1193G>C c.1568C>G (p.Thr523Arg) | |
7 | g.55181378C>T | CA090928 | EGFR,EGFR-AS1 | c.2210C>T (p.Thr737Met) c.718C>T c.2369C>T (p.Thr790Met) c.*28+8450C>T (n.*28+8450C>T) c.2234C>T (p.Thr745Met) n.1193G>A c.1568C>T (p.Thr523Met) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
7 | g.55181379G>A | CA4266062 | EGFR,EGFR-AS1 | c.2211G>A (p.Thr737=) c.719G>A c.2370G>A (p.Thr790=) c.*28+8451G>A (n.*28+8451G>A) c.2235G>A (p.Thr745=) n.1192C>T c.1569G>A (p.Thr523=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.55181379G>C | CA455165167 | EGFR,EGFR-AS1 | c.2211G>C (p.Thr737=) c.719G>C c.2370G>C (p.Thr790=) c.*28+8451G>C (n.*28+8451G>C) c.2235G>C (p.Thr745=) n.1192C>G c.1569G>C (p.Thr523=) | dbSNP |
7 | g.55181379G= | CA1708905494 | EGFR,EGFR-AS1 | c.2211G= (p.Thr737=) c.719G= c.2370G= (p.Thr790=) c.*28+8451G= (n.*28+8451G=) c.2235G= (p.Thr745=) n.1192C= c.1569G= (p.Thr523=) | |
7 | g.55181379G>T | CA455165168 | EGFR,EGFR-AS1 | c.2211G>T (p.Thr737=) c.719G>T c.2370G>T (p.Thr790=) c.*28+8451G>T (n.*28+8451G>T) c.2235G>T (p.Thr745=) n.1192C>A c.1569G>T (p.Thr523=) | ClinVar dbSNP |
7 | g.55181380C>A | CA367578856 | EGFR,EGFR-AS1 | c.2212C>A (p.Gln738Lys) c.720C>A c.2371C>A (p.Gln791Lys) c.*28+8452C>A (n.*28+8452C>A) c.2236C>A (p.Gln746Lys) n.1191G>T c.1570C>A (p.Gln524Lys) | gnomAD v4 |
7 | g.55181380C>G | CA367578855 | EGFR,EGFR-AS1 | c.2212C>G (p.Gln738Glu) c.720C>G c.2371C>G (p.Gln791Glu) c.*28+8452C>G (n.*28+8452C>G) c.2236C>G (p.Gln746Glu) n.1191G>C c.1570C>G (p.Gln524Glu) | dbSNP |
7 | g.55181380C>T | CA367578854 | EGFR,EGFR-AS1 | c.2212C>T (p.Gln738Ter) c.720C>T c.2371C>T (p.Gln791Ter) c.*28+8452C>T (n.*28+8452C>T) c.2236C>T (p.Gln746Ter) n.1191G>A c.1570C>T (p.Gln524Ter) | ClinVar dbSNP |
7 | g.55181381A>C | CA367578857 | EGFR,EGFR-AS1 | c.2213A>C (p.Gln738Pro) c.721A>C c.2372A>C (p.Gln791Pro) c.*28+8453A>C (n.*28+8453A>C) c.2237A>C (p.Gln746Pro) n.1190T>G c.1571A>C (p.Gln524Pro) | dbSNP |
7 | g.55181381A>G | CA367578858 | EGFR,EGFR-AS1 | c.2213A>G (p.Gln738Arg) c.721A>G c.2372A>G (p.Gln791Arg) c.*28+8453A>G (n.*28+8453A>G) c.2237A>G (p.Gln746Arg) n.1190T>C c.1571A>G (p.Gln524Arg) | gnomAD v4 |
7 | g.55181381A>T | CA367578859 | EGFR,EGFR-AS1 | c.2213A>T (p.Gln738Leu) c.721A>T c.2372A>T (p.Gln791Leu) c.*28+8453A>T (n.*28+8453A>T) c.2237A>T (p.Gln746Leu) n.1190T>A c.1571A>T (p.Gln524Leu) | dbSNP |
7 | g.55181382del | CA455165173 | EGFR,EGFR-AS1 | c.2214del (p.Gln738HisfsTer?) c.722del c.2373del (p.Gln791HisfsTer?) c.*28+8454del (n.*28+8454del) c.2238del (p.Gln746HisfsTer?) n.1189del c.1572del (p.Gln524HisfsTer?) | COSMIC |
7 | g.55181382G>A | CA455165172 | EGFR,EGFR-AS1 | c.2214G>A (p.Gln738=) c.722G>A c.2373G>A (p.Gln791=) c.*28+8454G>A (n.*28+8454G>A) c.2238G>A (p.Gln746=) n.1189C>T c.1572G>A (p.Gln524=) | dbSNP gnomAD v4 |
7 | g.55181382G>C | CA367578860 | EGFR,EGFR-AS1 | c.2214G>C (p.Gln738His) c.722G>C c.2373G>C (p.Gln791His) c.*28+8454G>C (n.*28+8454G>C) c.2238G>C (p.Gln746His) n.1189C>G c.1572G>C (p.Gln524His) | dbSNP |
7 | g.55181382G= | CA1708905501 | EGFR,EGFR-AS1 | c.2214G= (p.Gln738=) c.722G= c.2373G= (p.Gln791=) c.*28+8454G= (n.*28+8454G=) c.2238G= (p.Gln746=) n.1189C= c.1572G= (p.Gln524=) | |
7 | g.55181382G>T | CA367578861 | EGFR,EGFR-AS1 | c.2214G>T (p.Gln738His) c.722G>T c.2373G>T (p.Gln791His) c.*28+8454G>T (n.*28+8454G>T) c.2238G>T (p.Gln746His) n.1189C>A c.1572G>T (p.Gln524His) | ClinVar dbSNP gnomAD v2 |
7 | g.55181383C>A | CA367578862 | EGFR,EGFR-AS1 | c.2215C>A (p.Leu739Ile) c.723C>A c.2374C>A (p.Leu792Ile) c.*28+8455C>A (n.*28+8455C>A) c.2239C>A (p.Leu747Ile) n.1188G>T c.1573C>A (p.Leu525Ile) | dbSNP |
7 | g.55181383C>G | CA367578863 | EGFR,EGFR-AS1 | c.2215C>G (p.Leu739Val) c.723C>G c.2374C>G (p.Leu792Val) c.*28+8455C>G (n.*28+8455C>G) c.2239C>G (p.Leu747Val) n.1188G>C c.1573C>G (p.Leu525Val) | dbSNP |
7 | g.55181383C>T | CA367578864 | EGFR,EGFR-AS1 | c.2215C>T (p.Leu739Phe) c.723C>T c.2374C>T (p.Leu792Phe) c.*28+8455C>T (n.*28+8455C>T) c.2239C>T (p.Leu747Phe) n.1188G>A c.1573C>T (p.Leu525Phe) | ClinVar dbSNP gnomAD v4 |
7 | g.55181383_55181384delinsTA | CA2714937418 | EGFR,EGFR-AS1 | c.2215_2216delinsTA (p.Leu739Tyr) c.723_724delinsTA c.2374_2375delinsTA (p.Leu792Tyr) c.*28+8455_*28+8456delinsTA (n.*28+8455_*28+8456delinsTA) c.2239_2240delinsTA (p.Leu747Tyr) n.1187_1188delinsTA c.1573_1574delinsTA (p.Leu525Tyr) | dbSNP |
7 | g.55181384T>A | CA367578865 | EGFR,EGFR-AS1 | c.2216T>A (p.Leu739His) c.724T>A c.2375T>A (p.Leu792His) c.*28+8456T>A (n.*28+8456T>A) c.2240T>A (p.Leu747His) n.1187A>T c.1574T>A (p.Leu525His) | dbSNP |
7 | g.55181384T>C | CA367578866 | EGFR,EGFR-AS1 | c.2216T>C (p.Leu739Pro) c.724T>C c.2375T>C (p.Leu792Pro) c.*28+8456T>C (n.*28+8456T>C) c.2240T>C (p.Leu747Pro) n.1187A>G c.1574T>C (p.Leu525Pro) | dbSNP COSMIC |
7 | g.55181384T>G | CA367578867 | EGFR,EGFR-AS1 | c.2216T>G (p.Leu739Arg) c.724T>G c.2375T>G (p.Leu792Arg) c.*28+8456T>G (n.*28+8456T>G) c.2240T>G (p.Leu747Arg) n.1187A>C c.1574T>G (p.Leu525Arg) | dbSNP |
7 | g.55181385C>A | CA455165176 | EGFR,EGFR-AS1 | c.2217C>A (p.Leu739=) c.725C>A c.2376C>A (p.Leu792=) c.*28+8457C>A (n.*28+8457C>A) c.2241C>A (p.Leu747=) n.1186G>T c.1575C>A (p.Leu525=) | dbSNP |
7 | g.55181385C>G | CA455165177 | EGFR,EGFR-AS1 | c.2217C>G (p.Leu739=) c.725C>G c.2376C>G (p.Leu792=) c.*28+8457C>G (n.*28+8457C>G) c.2241C>G (p.Leu747=) n.1186G>C c.1575C>G (p.Leu525=) | COSMIC |
7 | g.55181385C>T | CA455165178 | EGFR,EGFR-AS1 | c.2217C>T (p.Leu739=) c.725C>T c.2376C>T (p.Leu792=) c.*28+8457C>T (n.*28+8457C>T) c.2241C>T (p.Leu747=) n.1186G>A c.1575C>T (p.Leu525=) | dbSNP |
7 | g.55181386A= | CA1708905509 | EGFR,EGFR-AS1 | c.2218A= (p.Met740=) c.726A= c.2377A= (p.Met793=) c.*28+8458A= (n.*28+8458A=) c.2242A= (p.Met748=) n.1185T= c.1576A= (p.Met526=) | |
7 | g.55181386A>C | CA367578868 | EGFR,EGFR-AS1 | c.2218A>C (p.Met740Leu) c.726A>C c.2377A>C (p.Met793Leu) c.*28+8458A>C (n.*28+8458A>C) c.2242A>C (p.Met748Leu) n.1185T>G c.1576A>C (p.Met526Leu) | gnomAD v4 |
7 | g.55181386A>G | CA367578869 | EGFR,EGFR-AS1 | c.2218A>G (p.Met740Val) c.726A>G c.2377A>G (p.Met793Val) c.*28+8458A>G (n.*28+8458A>G) c.2242A>G (p.Met748Val) n.1185T>C c.1576A>G (p.Met526Val) | dbSNP gnomAD v3 gnomAD v4 |
7 | g.55181386A>T | CA367578870 | EGFR,EGFR-AS1 | c.2218A>T (p.Met740Leu) c.726A>T c.2377A>T (p.Met793Leu) c.*28+8458A>T (n.*28+8458A>T) c.2242A>T (p.Met748Leu) n.1185T>A c.1576A>T (p.Met526Leu) | dbSNP |
7 | g.55181387T>A | CA367578872 | EGFR,EGFR-AS1 | c.2219T>A (p.Met740Lys) c.727T>A c.2378T>A (p.Met793Lys) c.*28+8459T>A (n.*28+8459T>A) c.2243T>A (p.Met748Lys) n.1184A>T c.1577T>A (p.Met526Lys) | dbSNP |
7 | g.55181387T>C | CA367578873 | EGFR,EGFR-AS1 | c.2219T>C (p.Met740Thr) c.727T>C c.2378T>C (p.Met793Thr) c.*28+8459T>C (n.*28+8459T>C) c.2243T>C (p.Met748Thr) n.1184A>G c.1577T>C (p.Met526Thr) | dbSNP gnomAD v4 |
7 | g.55181387T>G | CA367578871 | EGFR,EGFR-AS1 | c.2219T>G (p.Met740Arg) c.727T>G c.2378T>G (p.Met793Arg) c.*28+8459T>G (n.*28+8459T>G) c.2243T>G (p.Met748Arg) n.1184A>C c.1577T>G (p.Met526Arg) | dbSNP |
7 | g.55181388G>A | CA367578874 | EGFR,EGFR-AS1 | c.2220G>A (p.Met740Ile) c.728G>A c.2379G>A (p.Met793Ile) c.*28+8460G>A (n.*28+8460G>A) c.2244G>A (p.Met748Ile) n.1183C>T c.1578G>A (p.Met526Ile) | dbSNP |
7 | g.55181388G>C | CA367578875 | EGFR,EGFR-AS1 | c.2220G>C (p.Met740Ile) c.728G>C c.2379G>C (p.Met793Ile) c.*28+8460G>C (n.*28+8460G>C) c.2244G>C (p.Met748Ile) n.1183C>G c.1578G>C (p.Met526Ile) | |
7 | g.55181388G>T | CA367578876 | EGFR,EGFR-AS1 | c.2220G>T (p.Met740Ile) c.728G>T c.2379G>T (p.Met793Ile) c.*28+8460G>T (n.*28+8460G>T) c.2244G>T (p.Met748Ile) n.1183C>A c.1578G>T (p.Met526Ile) | COSMIC |
7 | g.55181389C>A | CA158928547 | EGFR,EGFR-AS1 | c.2221C>A (p.Pro741Thr) c.729C>A c.2380C>A (p.Pro794Thr) c.*28+8461C>A (n.*28+8461C>A) c.2245C>A (p.Pro749Thr) n.1182G>T c.1579C>A (p.Pro527Thr) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
7 | g.55181389C= | CA1708905514 | EGFR,EGFR-AS1 | c.2221C= (p.Pro741=) c.729C= c.2380C= (p.Pro794=) c.*28+8461C= (n.*28+8461C=) c.2245C= (p.Pro749=) n.1182G= c.1579C= (p.Pro527=) | |
7 | g.55181389C>G | CA367578877 | EGFR,EGFR-AS1 | c.2221C>G (p.Pro741Ala) c.729C>G c.2380C>G (p.Pro794Ala) c.*28+8461C>G (n.*28+8461C>G) c.2245C>G (p.Pro749Ala) n.1182G>C c.1579C>G (p.Pro527Ala) | dbSNP gnomAD v4 |
7 | g.55181389C>T | CA367578878 | EGFR,EGFR-AS1 | c.2221C>T (p.Pro741Ser) c.729C>T c.2380C>T (p.Pro794Ser) c.*28+8461C>T (n.*28+8461C>T) c.2245C>T (p.Pro749Ser) n.1182G>A c.1579C>T (p.Pro527Ser) | ClinVar dbSNP |
7 | g.55181390C>A | CA367578879 | EGFR,EGFR-AS1 | c.2222C>A (p.Pro741His) c.730C>A c.2381C>A (p.Pro794His) c.*28+8462C>A (n.*28+8462C>A) c.2246C>A (p.Pro749His) n.1181G>T c.1580C>A (p.Pro527His) | dbSNP COSMIC |
7 | g.55181390C>G | CA367578880 | EGFR,EGFR-AS1 | c.2222C>G (p.Pro741Arg) c.730C>G c.2381C>G (p.Pro794Arg) c.*28+8462C>G (n.*28+8462C>G) c.2246C>G (p.Pro749Arg) n.1181G>C c.1580C>G (p.Pro527Arg) | dbSNP |
7 | g.55181390C>T | CA367578881 | EGFR,EGFR-AS1 | c.2222C>T (p.Pro741Leu) c.730C>T c.2381C>T (p.Pro794Leu) c.*28+8462C>T (n.*28+8462C>T) c.2246C>T (p.Pro749Leu) n.1181G>A c.1580C>T (p.Pro527Leu) | dbSNP COSMIC |
7 | g.55181391C>A | CA455165188 | EGFR,EGFR-AS1 | c.2223C>A (p.Pro741=) c.731C>A c.2382C>A (p.Pro794=) c.*28+8463C>A (n.*28+8463C>A) c.2247C>A (p.Pro749=) n.1180G>T c.1581C>A (p.Pro527=) | gnomAD v4 |
7 | g.55181391C>G | CA455165187 | EGFR,EGFR-AS1 | c.2223C>G (p.Pro741=) c.731C>G c.2382C>G (p.Pro794=) c.*28+8463C>G (n.*28+8463C>G) c.2247C>G (p.Pro749=) n.1180G>C c.1581C>G (p.Pro527=) | |
7 | g.55181391C>T | CA455165185 | EGFR,EGFR-AS1 | c.2223C>T (p.Pro741=) c.731C>T c.2382C>T (p.Pro794=) c.*28+8463C>T (n.*28+8463C>T) c.2247C>T (p.Pro749=) n.1180G>A c.1581C>T (p.Pro527=) | gnomAD v4 |
7 | g.55181392T>A | CA367578882 | EGFR,EGFR-AS1 | c.2224T>A (p.Phe742Ile) c.732T>A c.2383T>A (p.Phe795Ile) c.*28+8464T>A (n.*28+8464T>A) c.2248T>A (p.Phe750Ile) n.1179A>T c.1582T>A (p.Phe528Ile) | dbSNP |
7 | g.55181392T>C | CA367578883 | EGFR,EGFR-AS1 | c.2224T>C (p.Phe742Leu) c.732T>C c.2383T>C (p.Phe795Leu) c.*28+8464T>C (n.*28+8464T>C) c.2248T>C (p.Phe750Leu) n.1179A>G c.1582T>C (p.Phe528Leu) | dbSNP |
7 | g.55181392T>G | CA367578884 | EGFR,EGFR-AS1 | c.2224T>G (p.Phe742Val) c.732T>G c.2383T>G (p.Phe795Val) c.*28+8464T>G (n.*28+8464T>G) c.2248T>G (p.Phe750Val) n.1179A>C c.1582T>G (p.Phe528Val) | gnomAD v4 |
7 | g.55181393T>A | CA367578887 | EGFR,EGFR-AS1 | c.2225T>A (p.Phe742Tyr) c.733T>A c.2384T>A (p.Phe795Tyr) c.*28+8465T>A (n.*28+8465T>A) c.2249T>A (p.Phe750Tyr) n.1178A>T c.1583T>A (p.Phe528Tyr) | dbSNP |
7 | g.55181393T>C | CA367578886 | EGFR,EGFR-AS1 | c.2225T>C (p.Phe742Ser) c.733T>C c.2384T>C (p.Phe795Ser) c.*28+8465T>C (n.*28+8465T>C) c.2249T>C (p.Phe750Ser) n.1178A>G c.1583T>C (p.Phe528Ser) | dbSNP COSMIC |
7 | g.55181393T>G | CA367578885 | EGFR,EGFR-AS1 | c.2225T>G (p.Phe742Cys) c.733T>G c.2384T>G (p.Phe795Cys) c.*28+8465T>G (n.*28+8465T>G) c.2249T>G (p.Phe750Cys) n.1178A>C c.1583T>G (p.Phe528Cys) | |
7 | g.55181394C>A | CA367578888 | EGFR,EGFR-AS1 | c.2226C>A (p.Phe742Leu) c.734C>A c.2385C>A (p.Phe795Leu) c.*28+8466C>A (n.*28+8466C>A) c.2250C>A (p.Phe750Leu) n.1177G>T c.1584C>A (p.Phe528Leu) | dbSNP gnomAD v4 |
7 | g.55181394C= | CA1708905518 | EGFR,EGFR-AS1 | c.2226C= (p.Phe742=) c.734C= c.2385C= (p.Phe795=) c.*28+8466C= (n.*28+8466C=) c.2250C= (p.Phe750=) n.1177G= c.1584C= (p.Phe528=) | |
7 | g.55181394C>G | CA367578889 | EGFR,EGFR-AS1 | c.2226C>G (p.Phe742Leu) c.734C>G c.2385C>G (p.Phe795Leu) c.*28+8466C>G (n.*28+8466C>G) c.2250C>G (p.Phe750Leu) n.1177G>C c.1584C>G (p.Phe528Leu) | dbSNP |
7 | g.55181394C>T | CA4266063 | EGFR,EGFR-AS1 | c.2226C>T (p.Phe742=) c.734C>T c.2385C>T (p.Phe795=) c.*28+8466C>T (n.*28+8466C>T) c.2250C>T (p.Phe750=) n.1177G>A c.1584C>T (p.Phe528=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |