Chr Mutation (hg38) CAid Gene Transcript Linkouts
7g.55174730G>ACA16602723EGFRc.2193G>A (p.Trp731Ter)
c.*28+1802G>A (p.=)
c.2058G>A (p.Trp686Ter)
c.2034G>A (p.Trp678Ter)
c.1392G>A (p.Trp464Ter)
ClinVar dbSNP COSMIC
7g.55174730G>CCA367583968EGFRc.2193G>C (p.Trp731Cys)
c.*28+1802G>C (p.=)
c.2058G>C (p.Trp686Cys)
c.2034G>C (p.Trp678Cys)
c.1392G>C (p.Trp464Cys)
7g.55174730G=CA1708918285EGFRc.2193G= (p.Trp731=)
c.*28+1802G= (p.=)
c.2058G= (p.Trp686=)
c.2034G= (p.Trp678=)
c.1392G= (p.Trp464=)
7g.55174730G>TCA367583970EGFRc.2193G>T (p.Trp731Cys)
c.*28+1802G>T (p.=)
c.2058G>T (p.Trp686Cys)
c.2034G>T (p.Trp678Cys)
c.1392G>T (p.Trp464Cys)
7g.55174731A>CCA367583973EGFRc.2194A>C (p.Ile732Leu)
c.*28+1803A>C (p.=)
c.2059A>C (p.Ile687Leu)
c.2035A>C (p.Ile679Leu)
c.1393A>C (p.Ile465Leu)
7g.55174731A>GCA367583974EGFRc.2194A>G (p.Ile732Val)
c.*28+1803A>G (p.=)
c.2059A>G (p.Ile687Val)
c.2035A>G (p.Ile679Val)
c.1393A>G (p.Ile465Val)
7g.55174731A>TCA367583975EGFRc.2194A>T (p.Ile732Phe)
c.*28+1803A>T (p.=)
c.2059A>T (p.Ile687Phe)
c.2035A>T (p.Ile679Phe)
c.1393A>T (p.Ile465Phe)
7g.55174732T>ACA367583978EGFRc.2195T>A (p.Ile732Asn)
c.*28+1804T>A (p.=)
c.2060T>A (p.Ile687Asn)
c.2036T>A (p.Ile679Asn)
c.1394T>A (p.Ile465Asn)
7g.55174732T>CCA367583980EGFRc.2195T>C (p.Ile732Thr)
c.*28+1804T>C (p.=)
c.2060T>C (p.Ile687Thr)
c.2036T>C (p.Ile679Thr)
c.1394T>C (p.Ile465Thr)
COSMIC
7g.55174732T>GCA367583981EGFRc.2195T>G (p.Ile732Ser)
c.*28+1804T>G (p.=)
c.2060T>G (p.Ile687Ser)
c.2036T>G (p.Ile679Ser)
c.1394T>G (p.Ile465Ser)
7g.55174733C>ACA454979273EGFRc.2196C>A (p.Ile732=)
c.*28+1805C>A (p.=)
c.2061C>A (p.Ile687=)
c.2037C>A (p.Ile679=)
c.1395C>A (p.Ile465=)
7g.55174733C>GCA367583982EGFRc.2196C>G (p.Ile732Met)
c.*28+1805C>G (p.=)
c.2061C>G (p.Ile687Met)
c.2037C>G (p.Ile679Met)
c.1395C>G (p.Ile465Met)
7g.55174733C>TCA454979276EGFRc.2196C>T (p.Ile732=)
c.*28+1805C>T (p.=)
c.2061C>T (p.Ile687=)
c.2037C>T (p.Ile679=)
c.1395C>T (p.Ile465=)
7g.55174734C>ACA367583987EGFRc.2197C>A (p.Pro733Thr)
c.*28+1806C>A (p.=)
c.2062C>A (p.Pro688Thr)
c.2038C>A (p.Pro680Thr)
c.1396C>A (p.Pro466Thr)
7g.55174734C=CA1708918286EGFRc.2197C= (p.Pro733=)
c.*28+1806C= (p.=)
c.2062C= (p.Pro688=)
c.2038C= (p.Pro680=)
c.1396C= (p.Pro466=)
7g.55174734C>GCA367583988EGFRc.2197C>G (p.Pro733Ala)
c.*28+1806C>G (p.=)
c.2062C>G (p.Pro688Ala)
c.2038C>G (p.Pro680Ala)
c.1396C>G (p.Pro466Ala)
7g.55174734C>TCA367583985EGFRc.2197C>T (p.Pro733Ser)
c.*28+1806C>T (p.=)
c.2062C>T (p.Pro688Ser)
c.2038C>T (p.Pro680Ser)
c.1396C>T (p.Pro466Ser)
COSMIC
7g.55174735C>ACA367583991EGFRc.2198C>A (p.Pro733Gln)
c.*28+1807C>A (p.=)
c.2063C>A (p.Pro688Gln)
c.2039C>A (p.Pro680Gln)
c.1397C>A (p.Pro466Gln)
7g.55174735C=CA1708918287EGFRc.2198C= (p.Pro733=)
c.*28+1807C= (p.=)
c.2063C= (p.Pro688=)
c.2039C= (p.Pro680=)
c.1397C= (p.Pro466=)
7g.55174735C>GCA367583993EGFRc.2198C>G (p.Pro733Arg)
c.*28+1807C>G (p.=)
c.2063C>G (p.Pro688Arg)
c.2039C>G (p.Pro680Arg)
c.1397C>G (p.Pro466Arg)
7g.55174735C>TCA16602538EGFRc.2198C>T (p.Pro733Leu)
c.*28+1807C>T (p.=)
c.2063C>T (p.Pro688Leu)
c.2039C>T (p.Pro680Leu)
c.1397C>T (p.Pro466Leu)
ClinVar dbSNP COSMIC
7g.55174736A>CCA454979284EGFRc.2199A>C (p.Pro733=)
c.*28+1808A>C (p.=)
c.2064A>C (p.Pro688=)
c.2040A>C (p.Pro680=)
c.1398A>C (p.Pro466=)
7g.55174736A>GCA454979285EGFRc.2199A>G (p.Pro733=)
c.*28+1808A>G (p.=)
c.2064A>G (p.Pro688=)
c.2040A>G (p.Pro680=)
c.1398A>G (p.Pro466=)
7g.55174736A>TCA454979287EGFRc.2199A>T (p.Pro733=)
c.*28+1808A>T (p.=)
c.2064A>T (p.Pro688=)
c.2040A>T (p.Pro680=)
c.1398A>T (p.Pro466=)
7g.55174737G>ACA16602539EGFRc.2200G>A (p.Glu734Lys)
c.*28+1809G>A (p.=)
c.2065G>A (p.Glu689Lys)
c.2041G>A (p.Glu681Lys)
c.1399G>A (p.Glu467Lys)
ClinVar dbSNP COSMIC
7g.55174737G>CCA367583997EGFRc.2200G>C (p.Glu734Gln)
c.*28+1809G>C (p.=)
c.2065G>C (p.Glu689Gln)
c.2041G>C (p.Glu681Gln)
c.1399G>C (p.Glu467Gln)
COSMIC
7g.55174737G=CA1708918288EGFRc.2200G= (p.Glu734=)
c.*28+1809G= (p.=)
c.2065G= (p.Glu689=)
c.2041G= (p.Glu681=)
c.1399G= (p.Glu467=)
7g.55174737G>TCA367583999EGFRc.2200G>T (p.Glu734Ter)
c.*28+1809G>T (p.=)
c.2065G>T (p.Glu689Ter)
c.2041G>T (p.Glu681Ter)
c.1399G>T (p.Glu467Ter)
7g.55174738A>CCA367584001EGFRc.2201A>C (p.Glu734Ala)
c.*28+1810A>C (p.=)
c.2066A>C (p.Glu689Ala)
c.2042A>C (p.Glu681Ala)
c.1400A>C (p.Glu467Ala)
7g.55174738A>GCA367584003EGFRc.2201A>G (p.Glu734Gly)
c.*28+1810A>G (p.=)
c.2066A>G (p.Glu689Gly)
c.2042A>G (p.Glu681Gly)
c.1400A>G (p.Glu467Gly)
COSMIC
7g.55174738A>TCA367584005EGFRc.2201A>T (p.Glu734Val)
c.*28+1810A>T (p.=)
c.2066A>T (p.Glu689Val)
c.2042A>T (p.Glu681Val)
c.1400A>T (p.Glu467Val)
7g.55174739A>CCA367584007EGFRc.2202A>C (p.Glu734Asp)
c.*28+1811A>C (p.=)
c.2067A>C (p.Glu689Asp)
c.2043A>C (p.Glu681Asp)
c.1401A>C (p.Glu467Asp)
7g.55174739A>GCA454979297EGFRc.2202A>G (p.Glu734=)
c.*28+1811A>G (p.=)
c.2067A>G (p.Glu689=)
c.2043A>G (p.Glu681=)
c.1401A>G (p.Glu467=)
7g.55174739A>TCA367584008EGFRc.2202A>T (p.Glu734Asp)
c.*28+1811A>T (p.=)
c.2067A>T (p.Glu689Asp)
c.2043A>T (p.Glu681Asp)
c.1401A>T (p.Glu467Asp)
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)

Number of alleles fetched