Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
7 | g.55181446T>A | CA367579000 | EGFR,EGFR-AS1 | c.2278T>A (p.Tyr760Asn) c.786T>A c.2437T>A (p.Tyr813Asn) c.*28+8518T>A (n.*28+8518T>A) c.2302T>A (p.Tyr768Asn) n.1125A>T c.1636T>A (p.Tyr546Asn) | dbSNP |
7 | g.55181446T>C | CA367579001 | EGFR,EGFR-AS1 | c.2278T>C (p.Tyr760His) c.786T>C c.2437T>C (p.Tyr813His) c.*28+8518T>C (n.*28+8518T>C) c.2302T>C (p.Tyr768His) n.1125A>G c.1636T>C (p.Tyr546His) | dbSNP gnomAD v4 |
7 | g.55181446T>G | CA367579002 | EGFR,EGFR-AS1 | c.2278T>G (p.Tyr760Asp) c.786T>G c.2437T>G (p.Tyr813Asp) c.*28+8518T>G (n.*28+8518T>G) c.2302T>G (p.Tyr768Asp) n.1125A>C c.1636T>G (p.Tyr546Asp) | dbSNP |
7 | g.55181447A>C | CA367579003 | EGFR,EGFR-AS1 | c.2279A>C (p.Tyr760Ser) c.787A>C c.2438A>C (p.Tyr813Ser) c.*28+8519A>C (n.*28+8519A>C) c.2303A>C (p.Tyr768Ser) n.1124T>G c.1637A>C (p.Tyr546Ser) | |
7 | g.55181447A>G | CA367579004 | EGFR,EGFR-AS1 | c.2279A>G (p.Tyr760Cys) c.787A>G c.2438A>G (p.Tyr813Cys) c.*28+8519A>G (n.*28+8519A>G) c.2303A>G (p.Tyr768Cys) n.1124T>C c.1637A>G (p.Tyr546Cys) | gnomAD v4 COSMIC |
7 | g.55181447A>T | CA367579005 | EGFR,EGFR-AS1 | c.2279A>T (p.Tyr760Phe) c.787A>T c.2438A>T (p.Tyr813Phe) c.*28+8519A>T (n.*28+8519A>T) c.2303A>T (p.Tyr768Phe) n.1124T>A c.1637A>T (p.Tyr546Phe) | |
7 | g.55181448C>A | CA367579006 | EGFR,EGFR-AS1 | c.2280C>A (p.Tyr760Ter) c.788C>A c.2439C>A (p.Tyr813Ter) c.*28+8520C>A (n.*28+8520C>A) c.2304C>A (p.Tyr768Ter) n.1123G>T c.1638C>A (p.Tyr546Ter) | dbSNP |
7 | g.55181448C= | CA1708905711 | EGFR,EGFR-AS1 | c.2280C= (p.Tyr760=) c.788C= c.2439C= (p.Tyr813=) c.*28+8520C= (n.*28+8520C=) c.2304C= (p.Tyr768=) n.1123G= c.1638C= (p.Tyr546=) | |
7 | g.55181448C>G | CA367579007 | EGFR,EGFR-AS1 | c.2280C>G (p.Tyr760Ter) c.788C>G c.2439C>G (p.Tyr813Ter) c.*28+8520C>G (n.*28+8520C>G) c.2304C>G (p.Tyr768Ter) n.1123G>C c.1638C>G (p.Tyr546Ter) | dbSNP |
7 | g.55181448C>T | CA135902 | EGFR,EGFR-AS1 | c.2280C>T (p.Tyr760=) c.788C>T c.2439C>T (p.Tyr813=) c.*28+8520C>T (n.*28+8520C>T) c.2304C>T (p.Tyr768=) n.1123G>A c.1638C>T (p.Tyr546=) | ClinVar dbSNP |
7 | g.55181449C>A | CA367579008 | EGFR,EGFR-AS1 | c.2281C>A (p.Leu761Met) c.789C>A c.2440C>A (p.Leu814Met) c.*28+8521C>A (n.*28+8521C>A) c.2305C>A (p.Leu769Met) n.1122G>T c.1639C>A (p.Leu547Met) | dbSNP |
7 | g.55181449C>G | CA367579009 | EGFR,EGFR-AS1 | c.2281C>G (p.Leu761Val) c.789C>G c.2440C>G (p.Leu814Val) c.*28+8521C>G (n.*28+8521C>G) c.2305C>G (p.Leu769Val) n.1122G>C c.1639C>G (p.Leu547Val) | dbSNP |
7 | g.55181449C>T | CA455165272 | EGFR,EGFR-AS1 | c.2281C>T (p.Leu761=) c.789C>T c.2440C>T (p.Leu814=) c.*28+8521C>T (n.*28+8521C>T) c.2305C>T (p.Leu769=) n.1122G>A c.1639C>T (p.Leu547=) | ClinVar dbSNP |
7 | g.55181450T>A | CA367579011 | EGFR,EGFR-AS1 | c.2282T>A (p.Leu761Gln) c.790T>A c.2441T>A (p.Leu814Gln) c.*28+8522T>A (n.*28+8522T>A) c.2306T>A (p.Leu769Gln) n.1121A>T c.1640T>A (p.Leu547Gln) | dbSNP |
7 | g.55181450T>C | CA367579012 | EGFR,EGFR-AS1 | c.2282T>C (p.Leu761Pro) c.790T>C c.2441T>C (p.Leu814Pro) c.*28+8522T>C (n.*28+8522T>C) c.2306T>C (p.Leu769Pro) n.1121A>G c.1640T>C (p.Leu547Pro) | ClinVar dbSNP |
7 | g.55181450T>G | CA367579010 | EGFR,EGFR-AS1 | c.2282T>G (p.Leu761Arg) c.790T>G c.2441T>G (p.Leu814Arg) c.*28+8522T>G (n.*28+8522T>G) c.2306T>G (p.Leu769Arg) n.1121A>C c.1640T>G (p.Leu547Arg) | gnomAD v4 |
7 | g.55181450T= | CA1708905721 | EGFR,EGFR-AS1 | c.2282T= (p.Leu761=) c.790T= c.2441T= (p.Leu814=) c.*28+8522T= (n.*28+8522T=) c.2306T= (p.Leu769=) n.1121A= c.1640T= (p.Leu547=) | |
7 | g.55181451G>A | CA455165275 | EGFR,EGFR-AS1 | c.2283G>A (p.Leu761=) c.791G>A c.2442G>A (p.Leu814=) c.*28+8523G>A (n.*28+8523G>A) c.2307G>A (p.Leu769=) n.1120C>T c.1641G>A (p.Leu547=) | dbSNP |
7 | g.55181451G>C | CA455165276 | EGFR,EGFR-AS1 | c.2283G>C (p.Leu761=) c.791G>C c.2442G>C (p.Leu814=) c.*28+8523G>C (n.*28+8523G>C) c.2307G>C (p.Leu769=) n.1120C>G c.1641G>C (p.Leu547=) | dbSNP |
7 | g.55181451G= | CA1708905732 | EGFR,EGFR-AS1 | c.2283G= (p.Leu761=) c.791G= c.2442G= (p.Leu814=) c.*28+8523G= (n.*28+8523G=) c.2307G= (p.Leu769=) n.1120C= c.1641G= (p.Leu547=) | |
7 | g.55181451G>T | CA4266071 | EGFR,EGFR-AS1 | c.2283G>T (p.Leu761=) c.791G>T c.2442G>T (p.Leu814=) c.*28+8523G>T (n.*28+8523G>T) c.2307G>T (p.Leu769=) n.1120C>A c.1641G>T (p.Leu547=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
7 | g.55181452C>A | CA367579013 | EGFR,EGFR-AS1 | c.2284C>A (p.Leu762Ile) c.792C>A c.2443C>A (p.Leu815Ile) c.*28+8524C>A (n.*28+8524C>A) c.2308C>A (p.Leu770Ile) n.1119G>T c.1642C>A (p.Leu548Ile) | dbSNP |
7 | g.55181452C= | CA1708905739 | EGFR,EGFR-AS1 | c.2284C= (p.Leu762=) c.792C= c.2443C= (p.Leu815=) c.*28+8524C= (n.*28+8524C=) c.2308C= (p.Leu770=) n.1119G= c.1642C= (p.Leu548=) | |
7 | g.55181452C>G | CA367579015 | EGFR,EGFR-AS1 | c.2284C>G (p.Leu762Val) c.792C>G c.2443C>G (p.Leu815Val) c.*28+8524C>G (n.*28+8524C>G) c.2308C>G (p.Leu770Val) n.1119G>C c.1642C>G (p.Leu548Val) | dbSNP |
7 | g.55181452C>T | CA367579014 | EGFR,EGFR-AS1 | c.2284C>T (p.Leu762Phe) c.792C>T c.2443C>T (p.Leu815Phe) c.*28+8524C>T (n.*28+8524C>T) c.2308C>T (p.Leu770Phe) n.1119G>A c.1642C>T (p.Leu548Phe) | dbSNP |
7 | g.55181453T>A | CA367579016 | EGFR,EGFR-AS1 | c.2285T>A (p.Leu762His) c.793T>A c.2444T>A (p.Leu815His) c.*28+8525T>A (n.*28+8525T>A) c.2309T>A (p.Leu770His) n.1118A>T c.1643T>A (p.Leu548His) | dbSNP |
7 | g.55181453T>C | CA367579017 | EGFR,EGFR-AS1 | c.2285T>C (p.Leu762Pro) c.793T>C c.2444T>C (p.Leu815Pro) c.*28+8525T>C (n.*28+8525T>C) c.2309T>C (p.Leu770Pro) n.1118A>G c.1643T>C (p.Leu548Pro) | |
7 | g.55181453T>G | CA367579018 | EGFR,EGFR-AS1 | c.2285T>G (p.Leu762Arg) c.793T>G c.2444T>G (p.Leu815Arg) c.*28+8525T>G (n.*28+8525T>G) c.2309T>G (p.Leu770Arg) n.1118A>C c.1643T>G (p.Leu548Arg) | |
7 | g.55181454C>A | CA455165280 | EGFR,EGFR-AS1 | c.2286C>A (p.Leu762=) c.794C>A c.2445C>A (p.Leu815=) c.*28+8526C>A (n.*28+8526C>A) c.2310C>A (p.Leu770=) n.1117G>T c.1644C>A (p.Leu548=) | dbSNP |
7 | g.55181454C>G | CA455165281 | EGFR,EGFR-AS1 | c.2286C>G (p.Leu762=) c.794C>G c.2445C>G (p.Leu815=) c.*28+8526C>G (n.*28+8526C>G) c.2310C>G (p.Leu770=) n.1117G>C c.1644C>G (p.Leu548=) | dbSNP |
7 | g.55181454C>T | CA455165279 | EGFR,EGFR-AS1 | c.2286C>T (p.Leu762=) c.794C>T c.2445C>T (p.Leu815=) c.*28+8526C>T (n.*28+8526C>T) c.2310C>T (p.Leu770=) n.1117G>A c.1644C>T (p.Leu548=) | ClinVar dbSNP COSMIC |
7 | g.55181455A= | CA1708905741 | EGFR,EGFR-AS1 | c.2287A= (p.Asn763=) c.795A= c.2446A= (p.Asn816=) c.*28+8527A= (n.*28+8527A=) c.2311A= (p.Asn771=) n.1116T= c.1645A= (p.Asn549=) | |
7 | g.55181455A>C | CA367579019 | EGFR,EGFR-AS1 | c.2287A>C (p.Asn763His) c.795A>C c.2446A>C (p.Asn816His) c.*28+8527A>C (n.*28+8527A>C) c.2311A>C (p.Asn771His) n.1116T>G c.1645A>C (p.Asn549His) | |
7 | g.55181455A>G | CA367579020 | EGFR,EGFR-AS1 | c.2287A>G (p.Asn763Asp) c.795A>G c.2446A>G (p.Asn816Asp) c.*28+8527A>G (n.*28+8527A>G) c.2311A>G (p.Asn771Asp) n.1116T>C c.1645A>G (p.Asn549Asp) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.55181455A>T | CA367579021 | EGFR,EGFR-AS1 | c.2287A>T (p.Asn763Tyr) c.795A>T c.2446A>T (p.Asn816Tyr) c.*28+8527A>T (n.*28+8527A>T) c.2311A>T (p.Asn771Tyr) n.1116T>A c.1645A>T (p.Asn549Tyr) | dbSNP |
7 | g.55181456A>C | CA367579022 | EGFR,EGFR-AS1 | c.2288A>C (p.Asn763Thr) c.796A>C c.2447A>C (p.Asn816Thr) c.*28+8528A>C (n.*28+8528A>C) c.2312A>C (p.Asn771Thr) n.1115T>G c.1646A>C (p.Asn549Thr) | ClinVar dbSNP |
7 | g.55181456A>G | CA367579023 | EGFR,EGFR-AS1 | c.2288A>G (p.Asn763Ser) c.796A>G c.2447A>G (p.Asn816Ser) c.*28+8528A>G (n.*28+8528A>G) c.2312A>G (p.Asn771Ser) n.1115T>C c.1646A>G (p.Asn549Ser) | ClinVar dbSNP |
7 | g.55181456A>T | CA367579024 | EGFR,EGFR-AS1 | c.2288A>T (p.Asn763Ile) c.796A>T c.2447A>T (p.Asn816Ile) c.*28+8528A>T (n.*28+8528A>T) c.2312A>T (p.Asn771Ile) n.1115T>A c.1646A>T (p.Asn549Ile) | dbSNP |
7 | g.55181457del | CA455165286 | EGFR,EGFR-AS1 | c.2289del (p.Trp764GlyfsTer9) c.797del c.2448del (p.Trp817GlyfsTer9) c.*28+8529del (n.*28+8529del) c.2313del (p.Trp772GlyfsTer9) n.1114del c.1647del (p.Trp550GlyfsTer9) | COSMIC |
7 | g.55181457C>A | CA367579025 | EGFR,EGFR-AS1 | c.2289C>A (p.Asn763Lys) c.797C>A c.2448C>A (p.Asn816Lys) c.*28+8529C>A (n.*28+8529C>A) c.2313C>A (p.Asn771Lys) n.1114G>T c.1647C>A (p.Asn549Lys) | |
7 | g.55181457C= | CA1708905788 | EGFR,EGFR-AS1 | c.2289C= (p.Asn763=) c.797C= c.2448C= (p.Asn816=) c.*28+8529C= (n.*28+8529C=) c.2313C= (p.Asn771=) n.1114G= c.1647C= (p.Asn549=) | |
7 | g.55181457C>G | CA367579026 | EGFR,EGFR-AS1 | c.2289C>G (p.Asn763Lys) c.797C>G c.2448C>G (p.Asn816Lys) c.*28+8529C>G (n.*28+8529C>G) c.2313C>G (p.Asn771Lys) n.1114G>C c.1647C>G (p.Asn549Lys) | dbSNP |
7 | g.55181457C>T | CA4266072 | EGFR,EGFR-AS1 | c.2289C>T (p.Asn763=) c.797C>T c.2448C>T (p.Asn816=) c.*28+8529C>T (n.*28+8529C>T) c.2313C>T (p.Asn771=) n.1114G>A c.1647C>T (p.Asn549=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.55181458T>A | CA367579027 | EGFR,EGFR-AS1 | c.2290T>A (p.Trp764Arg) c.798T>A c.2449T>A (p.Trp817Arg) c.*28+8530T>A (n.*28+8530T>A) c.2314T>A (p.Trp772Arg) n.1113A>T c.1648T>A (p.Trp550Arg) | |
7 | g.55181458T>C | CA367579029 | EGFR,EGFR-AS1 | c.2290T>C (p.Trp764Arg) c.798T>C c.2449T>C (p.Trp817Arg) c.*28+8530T>C (n.*28+8530T>C) c.2314T>C (p.Trp772Arg) n.1113A>G c.1648T>C (p.Trp550Arg) | |
7 | g.55181458T>G | CA367579028 | EGFR,EGFR-AS1 | c.2290T>G (p.Trp764Gly) c.798T>G c.2449T>G (p.Trp817Gly) c.*28+8530T>G (n.*28+8530T>G) c.2314T>G (p.Trp772Gly) n.1113A>C c.1648T>G (p.Trp550Gly) | |
7 | g.55181459G>A | CA367579030 | EGFR,EGFR-AS1 | c.2291G>A (p.Trp764Ter) c.799G>A c.2450G>A (p.Trp817Ter) c.*28+8531G>A (n.*28+8531G>A) c.2315G>A (p.Trp772Ter) n.1112C>T c.1649G>A (p.Trp550Ter) | dbSNP |
7 | g.55181459G>C | CA367579031 | EGFR,EGFR-AS1 | c.2291G>C (p.Trp764Ser) c.799G>C c.2450G>C (p.Trp817Ser) c.*28+8531G>C (n.*28+8531G>C) c.2315G>C (p.Trp772Ser) n.1112C>G c.1649G>C (p.Trp550Ser) | dbSNP |
7 | g.55181459G>T | CA367579032 | EGFR,EGFR-AS1 | c.2291G>T (p.Trp764Leu) c.799G>T c.2450G>T (p.Trp817Leu) c.*28+8531G>T (n.*28+8531G>T) c.2315G>T (p.Trp772Leu) n.1112C>A c.1649G>T (p.Trp550Leu) | dbSNP |
7 | g.55181459_55181460insAT | CA645561610 | EGFR,EGFR-AS1 | c.2291_2292insAT (p.Trp764Ter) c.799_800insAT c.2450_2451insAT (p.Trp817Ter) c.*28+8531_*28+8532insAT (n.*28+8531_*28+8532insAT) c.2315_2316insAT (p.Trp772Ter) n.1111_1112insAT c.1649_1650insAT (p.Trp550Ter) | COSMIC |