Chr Mutation (hg38) CAid Gene Transcript Linkouts
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)
7g.55181457C=CA1708905788EGFR,EGFR-AS1c.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=)
7g.55181457C>GCA367579026EGFR,EGFR-AS1c.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
7g.55181457C>TCA4266072EGFR,EGFR-AS1c.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
7g.55181458T>ACA367579027EGFR,EGFR-AS1c.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)
7g.55181458T>CCA367579029EGFR,EGFR-AS1c.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)
7g.55181458T>GCA367579028EGFR,EGFR-AS1c.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)
7g.55181459G>ACA367579030EGFR,EGFR-AS1c.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
7g.55181459G>CCA367579031EGFR,EGFR-AS1c.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
7g.55181459G>TCA367579032EGFR,EGFR-AS1c.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
7g.55181459_55181460insATCA645561610EGFR,EGFR-AS1c.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
7g.55181460G>ACA367579033EGFR,EGFR-AS1c.2292G>A (p.Trp764Ter)
c.800G>A
c.2451G>A (p.Trp817Ter)
c.*28+8532G>A (n.*28+8532G>A)
c.2316G>A (p.Trp772Ter)
n.1111C>T
c.1650G>A (p.Trp550Ter)
 dbSNP
7g.55181460G>CCA367579034EGFR,EGFR-AS1c.2292G>C (p.Trp764Cys)
c.800G>C
c.2451G>C (p.Trp817Cys)
c.*28+8532G>C (n.*28+8532G>C)
c.2316G>C (p.Trp772Cys)
n.1111C>G
c.1650G>C (p.Trp550Cys)
 dbSNP
7g.55181460G>TCA367579035EGFR,EGFR-AS1c.2292G>T (p.Trp764Cys)
c.800G>T
c.2451G>T (p.Trp817Cys)
c.*28+8532G>T (n.*28+8532G>T)
c.2316G>T (p.Trp772Cys)
n.1111C>A
c.1650G>T (p.Trp550Cys)
 dbSNP
7g.55181461T>ACA367579036EGFR,EGFR-AS1c.2293T>A (p.Cys765Ser)
c.801T>A
c.2452T>A (p.Cys818Ser)
c.*28+8533T>A (n.*28+8533T>A)
c.2317T>A (p.Cys773Ser)
n.1110A>T
c.1651T>A (p.Cys551Ser)
 dbSNP
7g.55181461T>CCA367579037EGFR,EGFR-AS1c.2293T>C (p.Cys765Arg)
c.801T>C
c.2452T>C (p.Cys818Arg)
c.*28+8533T>C (n.*28+8533T>C)
c.2317T>C (p.Cys773Arg)
n.1110A>G
c.1651T>C (p.Cys551Arg)
7g.55181461T>GCA367579038EGFR,EGFR-AS1c.2293T>G (p.Cys765Gly)
c.801T>G
c.2452T>G (p.Cys818Gly)
c.*28+8533T>G (n.*28+8533T>G)
c.2317T>G (p.Cys773Gly)
n.1110A>C
c.1651T>G (p.Cys551Gly)
 dbSNP
7g.55181462G>ACA367579040EGFR,EGFR-AS1c.2294G>A (p.Cys765Tyr)
c.802G>A
c.2453G>A (p.Cys818Tyr)
c.*28+8534G>A (n.*28+8534G>A)
c.2318G>A (p.Cys773Tyr)
n.1109C>T
c.1652G>A (p.Cys551Tyr)
 ClinVar dbSNP COSMIC
7g.55181462G>CCA367579041EGFR,EGFR-AS1c.2294G>C (p.Cys765Ser)
c.802G>C
c.2453G>C (p.Cys818Ser)
c.*28+8534G>C (n.*28+8534G>C)
c.2318G>C (p.Cys773Ser)
n.1109C>G
c.1652G>C (p.Cys551Ser)
 dbSNP
7g.55181462G>TCA367579039EGFR,EGFR-AS1c.2294G>T (p.Cys765Phe)
c.802G>T
c.2453G>T (p.Cys818Phe)
c.*28+8534G>T (n.*28+8534G>T)
c.2318G>T (p.Cys773Phe)
n.1109C>A
c.1652G>T (p.Cys551Phe)
 dbSNP
7g.55181463T>ACA367579042EGFR,EGFR-AS1c.2295T>A (p.Cys765Ter)
c.803T>A
c.2454T>A (p.Cys818Ter)
c.*28+8535T>A (n.*28+8535T>A)
c.2319T>A (p.Cys773Ter)
n.1108A>T
c.1653T>A (p.Cys551Ter)
 dbSNP

Number of alleles fetched