Chr Mutation (hg38) CAid Gene Transcript Linkouts
6g.64230597_64230598delCA2578660041EYSc.6418_6419del (p.Glu2140LysfsTer30)
6g.64230598C>ACA364391147EYSc.6418G>T (p.Glu2140Ter)
6g.64230598C>GCA364391149EYSc.6418G>C (p.Glu2140Gln)
6g.64230598C>TCA364391148EYSc.6418G>A (p.Glu2140Lys)
COSMIC
6g.64230599A>CCA364391150EYSc.6417T>G (p.Cys2139Trp)
6g.64230599A>GCA450758748EYSc.6417T>C (p.Cys2139=)
6g.64230599A>TCA364391151EYSc.6417T>A (p.Cys2139Ter)
6g.64230600C>ACA364391152EYSc.6416G>T (p.Cys2139Phe)
6g.64230600C=CA1633626627EYSc.6416G= (p.Cys2139=)
6g.64230600C>GCA364391153EYSc.6416G>C (p.Cys2139Ser)
6g.64230600C>TCA199162EYSc.6416G>A (p.Cys2139Tyr)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
6g.64230601A=CA1633626628EYSc.6415T= (p.Cys2139=)
6g.64230601A>CCA364391154EYSc.6415T>G (p.Cys2139Gly)
6g.64230601A>GCA364391155EYSc.6415T>C (p.Cys2139Arg)
ClinVar dbSNP
6g.64230601A>TCA364391156EYSc.6415T>A (p.Cys2139Ser)
6g.64230601_64230612delCA2679283466EYSc.6404_6415del (p.Thr2135_Cys2139delinsSer)
ClinVar gnomAD v4
6g.64230602G>ACA450758749EYSc.6414C>T (p.Phe2138=)
ClinVar gnomAD v4
6g.64230602G>CCA364391157EYSc.6414C>G (p.Phe2138Leu)
6g.64230602G>TCA364391158EYSc.6414C>A (p.Phe2138Leu)
6g.64230603A>CCA364391161EYSc.6413T>G (p.Phe2138Cys)
6g.64230603A>GCA364391160EYSc.6413T>C (p.Phe2138Ser)
gnomAD v4
6g.64230603A>TCA364391159EYSc.6413T>A (p.Phe2138Tyr)
6g.64230604A=CA1633626629EYSc.6412T= (p.Phe2138=)
6g.64230604A>CCA364391162EYSc.6412T>G (p.Phe2138Val)
6g.64230604A>GCA364391163EYSc.6412T>C (p.Phe2138Leu)
dbSNP gnomAD v2 gnomAD v4
6g.64230604A>TCA364391164EYSc.6412T>A (p.Phe2138Ile)
6g.64230605G>ACA450758752EYSc.6411C>T (p.Arg2137=)
6g.64230605G>CCA450758751EYSc.6411C>G (p.Arg2137=)
6g.64230605G>TCA450758750EYSc.6411C>A (p.Arg2137=)
6g.64230606C>ACA364391165EYSc.6410G>T (p.Arg2137Leu)
gnomAD v4
6g.64230606C=CA1633626630EYSc.6410G= (p.Arg2137=)
6g.64230606C>GCA364391166EYSc.6410G>C (p.Arg2137Pro)
6g.64230606C>TCA140296089EYSc.6410G>A (p.Arg2137His)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
6g.64230607G>ACA3876922EYSc.6409C>T (p.Arg2137Cys)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
6g.64230607G>CCA364391167EYSc.6409C>G (p.Arg2137Gly)
6g.64230607G=CA1633626631EYSc.6409C= (p.Arg2137=)
6g.64230607G>TCA364391168EYSc.6409C>A (p.Arg2137Ser)
6g.64230608G>ACA450758753EYSc.6408C>T (p.Gly2136=)
ClinVar
6g.64230608G>CCA450758754EYSc.6408C>G (p.Gly2136=)
gnomAD v4
6g.64230608G>TCA450758755EYSc.6408C>A (p.Gly2136=)
6g.64230609C>ACA364391169EYSc.6407G>T (p.Gly2136Val)
6g.64230609C=CA1633626632EYSc.6407G= (p.Gly2136=)
6g.64230609C>GCA364391170EYSc.6407G>C (p.Gly2136Ala)
ClinVar dbSNP gnomAD v3 gnomAD v4
6g.64230609C>TCA364391171EYSc.6407G>A (p.Gly2136Asp)
gnomAD v4
6g.64230610C>ACA364391173EYSc.6406G>T (p.Gly2136Cys)
6g.64230610C>GCA364391174EYSc.6406G>C (p.Gly2136Arg)
6g.64230610C>TCA364391172EYSc.6406G>A (p.Gly2136Ser)
6g.64230611A=CA1633626633EYSc.6405T= (p.Thr2135=)
6g.64230611A>CCA450758757EYSc.6405T>G (p.Thr2135=)
6g.64230611A>GCA450758758EYSc.6405T>C (p.Thr2135=)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4

Number of alleles fetched