Chr Mutation (hg38) CAid Gene Transcript Linkouts
7g.55174737G>ACA16602539EGFRc.2041G>A (p.Glu681Lys)
c.549G>A
c.2200G>A (p.Glu734Lys)
c.*28+1809G>A (n.*28+1809G>A)
c.2065G>A (p.Glu689Lys)
c.1399G>A (p.Glu467Lys)
ClinVar dbSNP gnomAD v4 COSMIC
7g.55174737G>CCA367583997EGFRc.2041G>C (p.Glu681Gln)
c.549G>C
c.2200G>C (p.Glu734Gln)
c.*28+1809G>C (n.*28+1809G>C)
c.2065G>C (p.Glu689Gln)
c.1399G>C (p.Glu467Gln)
COSMIC
7g.55174737G=CA1708918288EGFRc.2041G= (p.Glu681=)
c.549G=
c.2200G= (p.Glu734=)
c.*28+1809G= (n.*28+1809G=)
c.2065G= (p.Glu689=)
c.1399G= (p.Glu467=)
7g.55174737G>TCA367583999EGFRc.2041G>T (p.Glu681Ter)
c.549G>T
c.2200G>T (p.Glu734Ter)
c.*28+1809G>T (n.*28+1809G>T)
c.2065G>T (p.Glu689Ter)
c.1399G>T (p.Glu467Ter)
7g.55174738A>CCA367584001EGFRc.2042A>C (p.Glu681Ala)
c.550A>C
c.2201A>C (p.Glu734Ala)
c.*28+1810A>C (n.*28+1810A>C)
c.2066A>C (p.Glu689Ala)
c.1400A>C (p.Glu467Ala)
dbSNP
7g.55174738A>GCA367584003EGFRc.2042A>G (p.Glu681Gly)
c.550A>G
c.2201A>G (p.Glu734Gly)
c.*28+1810A>G (n.*28+1810A>G)
c.2066A>G (p.Glu689Gly)
c.1400A>G (p.Glu467Gly)
COSMIC
7g.55174738A>TCA367584005EGFRc.2042A>T (p.Glu681Val)
c.550A>T
c.2201A>T (p.Glu734Val)
c.*28+1810A>T (n.*28+1810A>T)
c.2066A>T (p.Glu689Val)
c.1400A>T (p.Glu467Val)
dbSNP
7g.55174739A>CCA367584007EGFRc.2043A>C (p.Glu681Asp)
c.551A>C
c.2202A>C (p.Glu734Asp)
c.*28+1811A>C (n.*28+1811A>C)
c.2067A>C (p.Glu689Asp)
c.1401A>C (p.Glu467Asp)
7g.55174739A>GCA454979297EGFRc.2043A>G (p.Glu681=)
c.551A>G
c.2202A>G (p.Glu734=)
c.*28+1811A>G (n.*28+1811A>G)
c.2067A>G (p.Glu689=)
c.1401A>G (p.Glu467=)
gnomAD v4
7g.55174739A>TCA367584008EGFRc.2043A>T (p.Glu681Asp)
c.551A>T
c.2202A>T (p.Glu734Asp)
c.*28+1811A>T (n.*28+1811A>T)
c.2067A>T (p.Glu689Asp)
c.1401A>T (p.Glu467Asp)
dbSNP
7g.55174740G>ACA16602540EGFRc.2044G>A (p.Gly682Ser)
c.552G>A
c.2203G>A (p.Gly735Ser)
c.*28+1812G>A (n.*28+1812G>A)
c.2068G>A (p.Gly690Ser)
c.1402G>A (p.Gly468Ser)
ClinVar dbSNP COSMIC
7g.55174740G>CCA367584012EGFRc.2044G>C (p.Gly682Arg)
c.552G>C
c.2203G>C (p.Gly735Arg)
c.*28+1812G>C (n.*28+1812G>C)
c.2068G>C (p.Gly690Arg)
c.1402G>C (p.Gly468Arg)
7g.55174740G=CA1708918289EGFRc.2044G= (p.Gly682=)
c.552G=
c.2203G= (p.Gly735=)
c.*28+1812G= (n.*28+1812G=)
c.2068G= (p.Gly690=)
c.1402G= (p.Gly468=)
7g.55174740G>TCA367584013EGFRc.2044G>T (p.Gly682Cys)
c.552G>T
c.2203G>T (p.Gly735Cys)
c.*28+1812G>T (n.*28+1812G>T)
c.2068G>T (p.Gly690Cys)
c.1402G>T (p.Gly468Cys)
7g.55174741G>ACA367584019EGFRc.2045G>A (p.Gly682Asp)
c.553G>A
c.2204G>A (p.Gly735Asp)
c.*28+1813G>A (n.*28+1813G>A)
c.2069G>A (p.Gly690Asp)
c.1403G>A (p.Gly468Asp)
dbSNP
7g.55174741G>CCA367584017EGFRc.2045G>C (p.Gly682Ala)
c.553G>C
c.2204G>C (p.Gly735Ala)
c.*28+1813G>C (n.*28+1813G>C)
c.2069G>C (p.Gly690Ala)
c.1403G>C (p.Gly468Ala)
dbSNP
7g.55174741G>TCA367584016EGFRc.2045G>T (p.Gly682Val)
c.553G>T
c.2204G>T (p.Gly735Val)
c.*28+1813G>T (n.*28+1813G>T)
c.2069G>T (p.Gly690Val)
c.1403G>T (p.Gly468Val)
7g.55174742T>ACA454979306EGFRc.2046T>A (p.Gly682=)
c.554T>A
c.2205T>A (p.Gly735=)
c.*28+1814T>A (n.*28+1814T>A)
c.2070T>A (p.Gly690=)
c.1404T>A (p.Gly468=)
dbSNP
7g.55174742T>CCA454979307EGFRc.2046T>C (p.Gly682=)
c.554T>C
c.2205T>C (p.Gly735=)
c.*28+1814T>C (n.*28+1814T>C)
c.2070T>C (p.Gly690=)
c.1404T>C (p.Gly468=)
ClinVar dbSNP gnomAD v4
7g.55174742T>GCA454979309EGFRc.2046T>G (p.Gly682=)
c.554T>G
c.2205T>G (p.Gly735=)
c.*28+1814T>G (n.*28+1814T>G)
c.2070T>G (p.Gly690=)
c.1404T>G (p.Gly468=)
dbSNP
7g.55174743G>ACA367584022EGFRc.2047G>A (p.Glu683Lys)
c.555G>A
c.2206G>A (p.Glu736Lys)
c.*28+1815G>A (n.*28+1815G>A)
c.2071G>A (p.Glu691Lys)
c.1405G>A (p.Glu469Lys)
ClinVar dbSNP
7g.55174743G>CCA367584023EGFRc.2047G>C (p.Glu683Gln)
c.555G>C
c.2206G>C (p.Glu736Gln)
c.*28+1815G>C (n.*28+1815G>C)
c.2071G>C (p.Glu691Gln)
c.1405G>C (p.Glu469Gln)
dbSNP
7g.55174743G=CA1708918290EGFRc.2047G= (p.Glu683=)
c.555G=
c.2206G= (p.Glu736=)
c.*28+1815G= (n.*28+1815G=)
c.2071G= (p.Glu691=)
c.1405G= (p.Glu469=)
7g.55174743G>TCA367584025EGFRc.2047G>T (p.Glu683Ter)
c.555G>T
c.2206G>T (p.Glu736Ter)
c.*28+1815G>T (n.*28+1815G>T)
c.2071G>T (p.Glu691Ter)
c.1405G>T (p.Glu469Ter)
dbSNP
7g.55174744A>CCA367584027EGFRc.2048A>C (p.Glu683Ala)
c.556A>C
c.2207A>C (p.Glu736Ala)
c.*28+1816A>C (n.*28+1816A>C)
c.2072A>C (p.Glu691Ala)
c.1406A>C (p.Glu469Ala)
7g.55174744A>GCA367584029EGFRc.2048A>G (p.Glu683Gly)
c.556A>G
c.2207A>G (p.Glu736Gly)
c.*28+1816A>G (n.*28+1816A>G)
c.2072A>G (p.Glu691Gly)
c.1406A>G (p.Glu469Gly)
7g.55174744A>TCA367584030EGFRc.2048A>T (p.Glu683Val)
c.556A>T
c.2207A>T (p.Glu736Val)
c.*28+1816A>T (n.*28+1816A>T)
c.2072A>T (p.Glu691Val)
c.1406A>T (p.Glu469Val)
dbSNP
7g.55174745G>ACA454979317EGFRc.2049G>A (p.Glu683=)
c.557G>A
c.2208G>A (p.Glu736=)
c.*28+1817G>A (n.*28+1817G>A)
c.2073G>A (p.Glu691=)
c.1407G>A (p.Glu469=)
ClinVar dbSNP
7g.55174745G>CCA367584033EGFRc.2049G>C (p.Glu683Asp)
c.557G>C
c.2208G>C (p.Glu736Asp)
c.*28+1817G>C (n.*28+1817G>C)
c.2073G>C (p.Glu691Asp)
c.1407G>C (p.Glu469Asp)
dbSNP
7g.55174745G>TCA367584034EGFRc.2049G>T (p.Glu683Asp)
c.557G>T
c.2208G>T (p.Glu736Asp)
c.*28+1817G>T (n.*28+1817G>T)
c.2073G>T (p.Glu691Asp)
c.1407G>T (p.Glu469Asp)
7g.55174746A>CCA367584037EGFRc.2050A>C (p.Lys684Gln)
c.558A>C
c.2209A>C (p.Lys737Gln)
c.*28+1818A>C (n.*28+1818A>C)
c.2074A>C (p.Lys692Gln)
c.1408A>C (p.Lys470Gln)
7g.55174746A>GCA367584039EGFRc.2050A>G (p.Lys684Glu)
c.558A>G
c.2209A>G (p.Lys737Glu)
c.*28+1818A>G (n.*28+1818A>G)
c.2074A>G (p.Lys692Glu)
c.1408A>G (p.Lys470Glu)
dbSNP COSMIC
7g.55174746A>TCA367584040EGFRc.2050A>T (p.Lys684Ter)
c.558A>T
c.2209A>T (p.Lys737Ter)
c.*28+1818A>T (n.*28+1818A>T)
c.2074A>T (p.Lys692Ter)
c.1408A>T (p.Lys470Ter)
dbSNP
7g.55174747A>CCA367584046EGFRc.2051A>C (p.Lys684Thr)
c.559A>C
c.2210A>C (p.Lys737Thr)
c.*28+1819A>C (n.*28+1819A>C)
c.2075A>C (p.Lys692Thr)
c.1409A>C (p.Lys470Thr)
7g.55174747A>GCA367584044EGFRc.2051A>G (p.Lys684Arg)
c.559A>G
c.2210A>G (p.Lys737Arg)
c.*28+1819A>G (n.*28+1819A>G)
c.2075A>G (p.Lys692Arg)
c.1409A>G (p.Lys470Arg)
dbSNP
7g.55174747A>TCA367584042EGFRc.2051A>T (p.Lys684Ile)
c.559A>T
c.2210A>T (p.Lys737Ile)
c.*28+1819A>T (n.*28+1819A>T)
c.2075A>T (p.Lys692Ile)
c.1409A>T (p.Lys470Ile)
dbSNP
7g.55174748A>CCA367584048EGFRc.2052A>C (p.Lys684Asn)
c.560A>C
c.2211A>C (p.Lys737Asn)
c.*28+1820A>C (n.*28+1820A>C)
c.2076A>C (p.Lys692Asn)
c.1410A>C (p.Lys470Asn)
7g.55174748A>GCA454979330EGFRc.2052A>G (p.Lys684=)
c.560A>G
c.2211A>G (p.Lys737=)
c.*28+1820A>G (n.*28+1820A>G)
c.2076A>G (p.Lys692=)
c.1410A>G (p.Lys470=)
ClinVar gnomAD v4
7g.55174748A>TCA367584049EGFRc.2052A>T (p.Lys684Asn)
c.560A>T
c.2211A>T (p.Lys737Asn)
c.*28+1820A>T (n.*28+1820A>T)
c.2076A>T (p.Lys692Asn)
c.1410A>T (p.Lys470Asn)
dbSNP
7g.55174749G>ACA367584052EGFRc.2053G>A (p.Val685Ile)
c.561G>A
c.2212G>A (p.Val738Ile)
c.*28+1821G>A (n.*28+1821G>A)
c.2077G>A (p.Val693Ile)
c.1411G>A (p.Val471Ile)
7g.55174749G>CCA367584053EGFRc.2053G>C (p.Val685Leu)
c.561G>C
c.2212G>C (p.Val738Leu)
c.*28+1821G>C (n.*28+1821G>C)
c.2077G>C (p.Val693Leu)
c.1411G>C (p.Val471Leu)
dbSNP
7g.55174749G>TCA367584056EGFRc.2053G>T (p.Val685Phe)
c.561G>T
c.2212G>T (p.Val738Phe)
c.*28+1821G>T (n.*28+1821G>T)
c.2077G>T (p.Val693Phe)
c.1411G>T (p.Val471Phe)
ClinVar dbSNP gnomAD v4
7g.55174750T>ACA367584060EGFRc.2054T>A (p.Val685Asp)
c.562T>A
c.2213T>A (p.Val738Asp)
c.*28+1822T>A (n.*28+1822T>A)
c.2078T>A (p.Val693Asp)
c.1412T>A (p.Val471Asp)
dbSNP
7g.55174750T>CCA367584059EGFRc.2054T>C (p.Val685Ala)
c.562T>C
c.2213T>C (p.Val738Ala)
c.*28+1822T>C (n.*28+1822T>C)
c.2078T>C (p.Val693Ala)
c.1412T>C (p.Val471Ala)
dbSNP gnomAD v2 gnomAD v4
7g.55174750T>GCA367584058EGFRc.2054T>G (p.Val685Gly)
c.562T>G
c.2213T>G (p.Val738Gly)
c.*28+1822T>G (n.*28+1822T>G)
c.2078T>G (p.Val693Gly)
c.1412T>G (p.Val471Gly)
dbSNP gnomAD v4 COSMIC
7g.55174750T=CA1708918291EGFRc.2054T= (p.Val685=)
c.562T=
c.2213T= (p.Val738=)
c.*28+1822T= (n.*28+1822T=)
c.2078T= (p.Val693=)
c.1412T= (p.Val471=)
7g.55174751_55174768dupCA645550319EGFRc.2055_2072dup (p.Ile691_Lys692insLysIleProValAlaIle)
c.563_580dup
c.2214_2231dup (p.Ile744_Lys745insLysIleProValAlaIle)
c.*28+1823_*28+1840dup (n.*28+1823_*28+1840dup)
c.2079_2096dup (p.Ile699_Lys700insLysIleProValAlaIle)
c.1413_1430dup (p.Ile477_Lys478insLysIleProValAlaIle)
dbSNP COSMIC COSMIC
7g.55174751T>ACA454979353EGFRc.2055T>A (p.Val685=)
c.563T>A
c.2214T>A (p.Val738=)
c.*28+1823T>A (n.*28+1823T>A)
c.2079T>A (p.Val693=)
c.1413T>A (p.Val471=)
gnomAD v4
7g.55174751T>CCA454979347EGFRc.2055T>C (p.Val685=)
c.563T>C
c.2214T>C (p.Val738=)
c.*28+1823T>C (n.*28+1823T>C)
c.2079T>C (p.Val693=)
c.1413T>C (p.Val471=)
7g.55174751T>GCA454979346EGFRc.2055T>G (p.Val685=)
c.563T>G
c.2214T>G (p.Val738=)
c.*28+1823T>G (n.*28+1823T>G)
c.2079T>G (p.Val693=)
c.1413T>G (p.Val471=)

Number of alleles fetched