Chr Mutation (hg38) CAid Gene Transcript Linkouts
7g.55181443C>ACA367578992EGFR,EGFR-AS1c.2275C>A (p.Gln759Lys)
c.783C>A
c.2434C>A (p.Gln812Lys)
c.*28+8515C>A (n.*28+8515C>A)
c.2299C>A (p.Gln767Lys)
n.1128G>T
c.1633C>A (p.Gln545Lys)
 dbSNP
7g.55181443C>GCA367578993EGFR,EGFR-AS1c.2275C>G (p.Gln759Glu)
c.783C>G
c.2434C>G (p.Gln812Glu)
c.*28+8515C>G (n.*28+8515C>G)
c.2299C>G (p.Gln767Glu)
n.1128G>C
c.1633C>G (p.Gln545Glu)
 dbSNP
7g.55181443C>TCA367578994EGFR,EGFR-AS1c.2275C>T (p.Gln759Ter)
c.783C>T
c.2434C>T (p.Gln812Ter)
c.*28+8515C>T (n.*28+8515C>T)
c.2299C>T (p.Gln767Ter)
n.1128G>A
c.1633C>T (p.Gln545Ter)
 dbSNP
7g.55181444A=CA1708905707EGFR,EGFR-AS1c.2276A= (p.Gln759=)
c.784A=
c.2435A= (p.Gln812=)
c.*28+8516A= (n.*28+8516A=)
c.2300A= (p.Gln767=)
n.1127T=
c.1634A= (p.Gln545=)
7g.55181444A>CCA367578997EGFR,EGFR-AS1c.2276A>C (p.Gln759Pro)
c.784A>C
c.2435A>C (p.Gln812Pro)
c.*28+8516A>C (n.*28+8516A>C)
c.2300A>C (p.Gln767Pro)
n.1127T>G
c.1634A>C (p.Gln545Pro)
 dbSNP
7g.55181444A>GCA367578995EGFR,EGFR-AS1c.2276A>G (p.Gln759Arg)
c.784A>G
c.2435A>G (p.Gln812Arg)
c.*28+8516A>G (n.*28+8516A>G)
c.2300A>G (p.Gln767Arg)
n.1127T>C
c.1634A>G (p.Gln545Arg)
 ClinVar gnomAD v4
7g.55181444A>TCA367578996EGFR,EGFR-AS1c.2276A>T (p.Gln759Leu)
c.784A>T
c.2435A>T (p.Gln812Leu)
c.*28+8516A>T (n.*28+8516A>T)
c.2300A>T (p.Gln767Leu)
n.1127T>A
c.1634A>T (p.Gln545Leu)
 dbSNP
7g.55181445G>ACA455165270EGFR,EGFR-AS1c.2277G>A (p.Gln759=)
c.785G>A
c.2436G>A (p.Gln812=)
c.*28+8517G>A (n.*28+8517G>A)
c.2301G>A (p.Gln767=)
n.1126C>T
c.1635G>A (p.Gln545=)
 ClinVar dbSNP
7g.55181445G>CCA367578998EGFR,EGFR-AS1c.2277G>C (p.Gln759His)
c.785G>C
c.2436G>C (p.Gln812His)
c.*28+8517G>C (n.*28+8517G>C)
c.2301G>C (p.Gln767His)
n.1126C>G
c.1635G>C (p.Gln545His)
 dbSNP gnomAD v4
7g.55181445G>TCA367578999EGFR,EGFR-AS1c.2277G>T (p.Gln759His)
c.785G>T
c.2436G>T (p.Gln812His)
c.*28+8517G>T (n.*28+8517G>T)
c.2301G>T (p.Gln767His)
n.1126C>A
c.1635G>T (p.Gln545His)
7g.55181446T>ACA367579000EGFR,EGFR-AS1c.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
7g.55181446T>CCA367579001EGFR,EGFR-AS1c.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
7g.55181446T>GCA367579002EGFR,EGFR-AS1c.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
7g.55181447A>CCA367579003EGFR,EGFR-AS1c.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)
7g.55181447A>GCA367579004EGFR,EGFR-AS1c.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
7g.55181447A>TCA367579005EGFR,EGFR-AS1c.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)
7g.55181448C>ACA367579006EGFR,EGFR-AS1c.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
7g.55181448C=CA1708905711EGFR,EGFR-AS1c.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=)
7g.55181448C>GCA367579007EGFR,EGFR-AS1c.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
7g.55181448C>TCA135902EGFR,EGFR-AS1c.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
7g.55181449C>ACA367579008EGFR,EGFR-AS1c.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
7g.55181449C>GCA367579009EGFR,EGFR-AS1c.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
7g.55181449C>TCA455165272EGFR,EGFR-AS1c.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
7g.55181450T>ACA367579011EGFR,EGFR-AS1c.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
7g.55181450T>CCA367579012EGFR,EGFR-AS1c.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
7g.55181450T>GCA367579010EGFR,EGFR-AS1c.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
7g.55181450T=CA1708905721EGFR,EGFR-AS1c.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=)
7g.55181451G>ACA455165275EGFR,EGFR-AS1c.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
7g.55181451G>CCA455165276EGFR,EGFR-AS1c.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
7g.55181451G=CA1708905732EGFR,EGFR-AS1c.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=)
7g.55181451G>TCA4266071EGFR,EGFR-AS1c.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
7g.55181452C>ACA367579013EGFR,EGFR-AS1c.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
7g.55181452C=CA1708905739EGFR,EGFR-AS1c.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=)
7g.55181452C>GCA367579015EGFR,EGFR-AS1c.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
7g.55181452C>TCA367579014EGFR,EGFR-AS1c.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
7g.55181453T>ACA367579016EGFR,EGFR-AS1c.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
7g.55181453T>CCA367579017EGFR,EGFR-AS1c.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)
7g.55181453T>GCA367579018EGFR,EGFR-AS1c.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)
7g.55181454C>ACA455165280EGFR,EGFR-AS1c.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
7g.55181454C>GCA455165281EGFR,EGFR-AS1c.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
7g.55181454C>TCA455165279EGFR,EGFR-AS1c.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
7g.55181455A=CA1708905741EGFR,EGFR-AS1c.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=)
7g.55181455A>CCA367579019EGFR,EGFR-AS1c.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)
7g.55181455A>GCA367579020EGFR,EGFR-AS1c.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
7g.55181455A>TCA367579021EGFR,EGFR-AS1c.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
7g.55181456A>CCA367579022EGFR,EGFR-AS1c.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
7g.55181456A>GCA367579023EGFR,EGFR-AS1c.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
7g.55181456A>TCA367579024EGFR,EGFR-AS1c.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
7g.55181457delCA455165286EGFR,EGFR-AS1c.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
7g.55181457C>ACA367579025EGFR,EGFR-AS1c.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)

Number of alleles fetched