Chr Mutation (hg38) CAid Gene Transcript Linkouts
7g.55174740G>ACA16602540EGFRc.2203G>A (p.Gly735Ser)
c.*28+1812G>A (p.=)
c.2068G>A (p.Gly690Ser)
c.2044G>A (p.Gly682Ser)
c.1402G>A (p.Gly468Ser)
ClinVar dbSNP COSMIC
7g.55174740G>CCA367584012EGFRc.2203G>C (p.Gly735Arg)
c.*28+1812G>C (p.=)
c.2068G>C (p.Gly690Arg)
c.2044G>C (p.Gly682Arg)
c.1402G>C (p.Gly468Arg)
7g.55174740G=CA1708918289EGFRc.2203G= (p.Gly735=)
c.*28+1812G= (p.=)
c.2068G= (p.Gly690=)
c.2044G= (p.Gly682=)
c.1402G= (p.Gly468=)
7g.55174740G>TCA367584013EGFRc.2203G>T (p.Gly735Cys)
c.*28+1812G>T (p.=)
c.2068G>T (p.Gly690Cys)
c.2044G>T (p.Gly682Cys)
c.1402G>T (p.Gly468Cys)
7g.55174741G>ACA367584019EGFRc.2204G>A (p.Gly735Asp)
c.*28+1813G>A (p.=)
c.2069G>A (p.Gly690Asp)
c.2045G>A (p.Gly682Asp)
c.1403G>A (p.Gly468Asp)
7g.55174741G>CCA367584017EGFRc.2204G>C (p.Gly735Ala)
c.*28+1813G>C (p.=)
c.2069G>C (p.Gly690Ala)
c.2045G>C (p.Gly682Ala)
c.1403G>C (p.Gly468Ala)
7g.55174741G>TCA367584016EGFRc.2204G>T (p.Gly735Val)
c.*28+1813G>T (p.=)
c.2069G>T (p.Gly690Val)
c.2045G>T (p.Gly682Val)
c.1403G>T (p.Gly468Val)
7g.55174742T>ACA454979306EGFRc.2205T>A (p.Gly735=)
c.*28+1814T>A (p.=)
c.2070T>A (p.Gly690=)
c.2046T>A (p.Gly682=)
c.1404T>A (p.Gly468=)
7g.55174742T>CCA454979307EGFRc.2205T>C (p.Gly735=)
c.*28+1814T>C (p.=)
c.2070T>C (p.Gly690=)
c.2046T>C (p.Gly682=)
c.1404T>C (p.Gly468=)
7g.55174742T>GCA454979309EGFRc.2205T>G (p.Gly735=)
c.*28+1814T>G (p.=)
c.2070T>G (p.Gly690=)
c.2046T>G (p.Gly682=)
c.1404T>G (p.Gly468=)
7g.55174743G>ACA367584022EGFRc.2206G>A (p.Glu736Lys)
c.*28+1815G>A (p.=)
c.2071G>A (p.Glu691Lys)
c.2047G>A (p.Glu683Lys)
c.1405G>A (p.Glu469Lys)
ClinVar
7g.55174743G>CCA367584023EGFRc.2206G>C (p.Glu736Gln)
c.*28+1815G>C (p.=)
c.2071G>C (p.Glu691Gln)
c.2047G>C (p.Glu683Gln)
c.1405G>C (p.Glu469Gln)
7g.55174743G=CA1708918290EGFRc.2206G= (p.Glu736=)
c.*28+1815G= (p.=)
c.2071G= (p.Glu691=)
c.2047G= (p.Glu683=)
c.1405G= (p.Glu469=)
7g.55174743G>TCA367584025EGFRc.2206G>T (p.Glu736Ter)
c.*28+1815G>T (p.=)
c.2071G>T (p.Glu691Ter)
c.2047G>T (p.Glu683Ter)
c.1405G>T (p.Glu469Ter)
7g.55174744A>CCA367584027EGFRc.2207A>C (p.Glu736Ala)
c.*28+1816A>C (p.=)
c.2072A>C (p.Glu691Ala)
c.2048A>C (p.Glu683Ala)
c.1406A>C (p.Glu469Ala)
7g.55174744A>GCA367584029EGFRc.2207A>G (p.Glu736Gly)
c.*28+1816A>G (p.=)
c.2072A>G (p.Glu691Gly)
c.2048A>G (p.Glu683Gly)
c.1406A>G (p.Glu469Gly)
7g.55174744A>TCA367584030EGFRc.2207A>T (p.Glu736Val)
c.*28+1816A>T (p.=)
c.2072A>T (p.Glu691Val)
c.2048A>T (p.Glu683Val)
c.1406A>T (p.Glu469Val)
7g.55174745G>ACA454979317EGFRc.2208G>A (p.Glu736=)
c.*28+1817G>A (p.=)
c.2073G>A (p.Glu691=)
c.2049G>A (p.Glu683=)
c.1407G>A (p.Glu469=)
7g.55174745G>CCA367584033EGFRc.2208G>C (p.Glu736Asp)
c.*28+1817G>C (p.=)
c.2073G>C (p.Glu691Asp)
c.2049G>C (p.Glu683Asp)
c.1407G>C (p.Glu469Asp)
7g.55174745G>TCA367584034EGFRc.2208G>T (p.Glu736Asp)
c.*28+1817G>T (p.=)
c.2073G>T (p.Glu691Asp)
c.2049G>T (p.Glu683Asp)
c.1407G>T (p.Glu469Asp)
7g.55174746A>CCA367584037EGFRc.2209A>C (p.Lys737Gln)
c.*28+1818A>C (p.=)
c.2074A>C (p.Lys692Gln)
c.2050A>C (p.Lys684Gln)
c.1408A>C (p.Lys470Gln)
7g.55174746A>GCA367584039EGFRc.2209A>G (p.Lys737Glu)
c.*28+1818A>G (p.=)
c.2074A>G (p.Lys692Glu)
c.2050A>G (p.Lys684Glu)
c.1408A>G (p.Lys470Glu)
COSMIC
7g.55174746A>TCA367584040EGFRc.2209A>T (p.Lys737Ter)
c.*28+1818A>T (p.=)
c.2074A>T (p.Lys692Ter)
c.2050A>T (p.Lys684Ter)
c.1408A>T (p.Lys470Ter)
7g.55174747A>CCA367584046EGFRc.2210A>C (p.Lys737Thr)
c.*28+1819A>C (p.=)
c.2075A>C (p.Lys692Thr)
c.2051A>C (p.Lys684Thr)
c.1409A>C (p.Lys470Thr)
7g.55174747A>GCA367584044EGFRc.2210A>G (p.Lys737Arg)
c.*28+1819A>G (p.=)
c.2075A>G (p.Lys692Arg)
c.2051A>G (p.Lys684Arg)
c.1409A>G (p.Lys470Arg)
7g.55174747A>TCA367584042EGFRc.2210A>T (p.Lys737Ile)
c.*28+1819A>T (p.=)
c.2075A>T (p.Lys692Ile)
c.2051A>T (p.Lys684Ile)
c.1409A>T (p.Lys470Ile)
7g.55174748A>CCA367584048EGFRc.2211A>C (p.Lys737Asn)
c.*28+1820A>C (p.=)
c.2076A>C (p.Lys692Asn)
c.2052A>C (p.Lys684Asn)
c.1410A>C (p.Lys470Asn)
7g.55174748A>GCA454979330EGFRc.2211A>G (p.Lys737=)
c.*28+1820A>G (p.=)
c.2076A>G (p.Lys692=)
c.2052A>G (p.Lys684=)
c.1410A>G (p.Lys470=)
7g.55174748A>TCA367584049EGFRc.2211A>T (p.Lys737Asn)
c.*28+1820A>T (p.=)
c.2076A>T (p.Lys692Asn)
c.2052A>T (p.Lys684Asn)
c.1410A>T (p.Lys470Asn)
7g.55174749G>ACA367584052EGFRc.2212G>A (p.Val738Ile)
c.*28+1821G>A (p.=)
c.2077G>A (p.Val693Ile)
c.2053G>A (p.Val685Ile)
c.1411G>A (p.Val471Ile)
7g.55174749G>CCA367584053EGFRc.2212G>C (p.Val738Leu)
c.*28+1821G>C (p.=)
c.2077G>C (p.Val693Leu)
c.2053G>C (p.Val685Leu)
c.1411G>C (p.Val471Leu)
7g.55174749G>TCA367584056EGFRc.2212G>T (p.Val738Phe)
c.*28+1821G>T (p.=)
c.2077G>T (p.Val693Phe)
c.2053G>T (p.Val685Phe)
c.1411G>T (p.Val471Phe)
7g.55174750T>ACA367584060EGFRc.2213T>A (p.Val738Asp)
c.*28+1822T>A (p.=)
c.2078T>A (p.Val693Asp)
c.2054T>A (p.Val685Asp)
c.1412T>A (p.Val471Asp)
7g.55174750T>CCA367584059EGFRc.2213T>C (p.Val738Ala)
c.*28+1822T>C (p.=)
c.2078T>C (p.Val693Ala)
c.2054T>C (p.Val685Ala)
c.1412T>C (p.Val471Ala)
gnomAD
7g.55174750T>GCA367584058EGFRc.2213T>G (p.Val738Gly)
c.*28+1822T>G (p.=)
c.2078T>G (p.Val693Gly)
c.2054T>G (p.Val685Gly)
c.1412T>G (p.Val471Gly)
COSMIC
7g.55174750T=CA1708918291EGFRc.2213T= (p.Val738=)
c.*28+1822T= (p.=)
c.2078T= (p.Val693=)
c.2054T= (p.Val685=)
c.1412T= (p.Val471=)
7g.55174751_55174768dupCA645550319EGFRc.2214_2231dup (p.Ile744_Lys745insLysIleProValAlaIle)
c.*28+1823_*28+1840dup (p.=)
c.2079_2096dup (p.Ile699_Lys700insLysIleProValAlaIle)
c.2055_2072dup (p.Ile691_Lys692insLysIleProValAlaIle)
c.1413_1430dup (p.Ile477_Lys478insLysIleProValAlaIle)
COSMIC COSMIC
7g.55174751T>ACA454979353EGFRc.2214T>A (p.Val738=)
c.*28+1823T>A (p.=)
c.2079T>A (p.Val693=)
c.2055T>A (p.Val685=)
c.1413T>A (p.Val471=)
7g.55174751T>CCA454979347EGFRc.2214T>C (p.Val738=)
c.*28+1823T>C (p.=)
c.2079T>C (p.Val693=)
c.2055T>C (p.Val685=)
c.1413T>C (p.Val471=)
7g.55174751T>GCA454979346EGFRc.2214T>G (p.Val738=)
c.*28+1823T>G (p.=)
c.2079T>G (p.Val693=)
c.2055T>G (p.Val685=)
c.1413T>G (p.Val471=)
7g.55174751T=CA1708918292EGFRc.2214T= (p.Val738=)
c.*28+1823T= (p.=)
c.2079T= (p.Val693=)
c.2055T= (p.Val685=)
c.1413T= (p.Val471=)
7g.55174752A>CCA367584063EGFRc.2215A>C (p.Lys739Gln)
c.*28+1824A>C (p.=)
c.2080A>C (p.Lys694Gln)
c.2056A>C (p.Lys686Gln)
c.1414A>C (p.Lys472Gln)
7g.55174752A>GCA367584065EGFRc.2215A>G (p.Lys739Glu)
c.*28+1824A>G (p.=)
c.2080A>G (p.Lys694Glu)
c.2056A>G (p.Lys686Glu)
c.1414A>G (p.Lys472Glu)
7g.55174752A>TCA367584066EGFRc.2215A>T (p.Lys739Ter)
c.*28+1824A>T (p.=)
c.2080A>T (p.Lys694Ter)
c.2056A>T (p.Lys686Ter)
c.1414A>T (p.Lys472Ter)
7g.55174755delCA645550320EGFRc.2218del (p.Ile740PhefsTer8)
c.*28+1827del (p.=)
c.2083del (p.Ile695PhefsTer8)
c.2059del (p.Ile687PhefsTer8)
c.1417del (p.Ile473PhefsTer8)
COSMIC
7g.55174754_55174771dupCA135785EGFRc.2217_2234dup (p.Lys745_Glu746insIleProValAlaIleLys)
c.*28+1826_*28+1843dup (p.=)
c.2082_2099dup (p.Lys700_Glu701insIleProValAlaIleLys)
c.2058_2075dup (p.Lys692_Glu693insIleProValAlaIleLys)
c.1416_1433dup (p.Lys478_Glu479insIleProValAlaIleLys)
ClinVar dbSNP dbSNP COSMIC COSMIC
7g.55174753A>CCA367584070EGFRc.2216A>C (p.Lys739Thr)
c.*28+1825A>C (p.=)
c.2081A>C (p.Lys694Thr)
c.2057A>C (p.Lys686Thr)
c.1415A>C (p.Lys472Thr)
7g.55174753A>GCA367584071EGFRc.2216A>G (p.Lys739Arg)
c.*28+1825A>G (p.=)
c.2081A>G (p.Lys694Arg)
c.2057A>G (p.Lys686Arg)
c.1415A>G (p.Lys472Arg)
7g.55174753A>TCA367584073EGFRc.2216A>T (p.Lys739Ile)
c.*28+1825A>T (p.=)
c.2081A>T (p.Lys694Ile)
c.2057A>T (p.Lys686Ile)
c.1415A>T (p.Lys472Ile)
7g.55174754A=CA1708918293EGFRc.2217A= (p.Lys739=)
c.*28+1826A= (p.=)
c.2082A= (p.Lys694=)
c.2058A= (p.Lys686=)
c.1416A= (p.Lys472=)

Number of alleles fetched