UPDATE - Protein Allele ID & Protein Sequence HGVS Requests Partially Restored
Protein allele requests are no longer disabled.
Currently, hypothetical explanatory transcript generation is not part of the response and is being investigated.
Protein allele requests are no longer disabled.
Currently, hypothetical explanatory transcript generation is not part of the response and is being investigated.
| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 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.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.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.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.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.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=) |