Chr Mutation (hg38) CAid Gene Transcript Linkouts
6g.49457753A=CA1627392091MMUTc.691T= (p.Tyr231=)
6g.49457753A>CCA364404070MMUTc.691T>G (p.Tyr231Asp)
6g.49457753A>GCA364404073MMUTc.691T>C (p.Tyr231His)
6g.49457753A>TCA347881MMUTc.691T>A (p.Tyr231Asn)
ClinVar dbSNP gnomAD v3 gnomAD v4
6g.49457754T>ACA450608767MMUTc.690A>T (p.Thr230=)
dbSNP
6g.49457754T>CCA450608768MMUTc.690A>G (p.Thr230=)
ClinVar gnomAD v4 COSMIC
6g.49457754T>GCA450608769MMUTc.690A>C (p.Thr230=)
6g.49457754T=CA1627392092MMUTc.690A= (p.Thr230=)
6g.49457755_49457756delCA2499218332MMUTc.689_690del (p.Thr230IlefsTer14)
ClinVar dbSNP
6g.49457755G>ACA364404076MMUTc.689C>T (p.Thr230Ile)
ClinVar dbSNP
6g.49457755G>CCA10575878MMUTc.689C>G (p.Thr230Arg)
ClinVar dbSNP gnomAD v4
6g.49457755G=CA1627392093MMUTc.689C= (p.Thr230=)
6g.49457755G>TCA364404077MMUTc.689C>A (p.Thr230Lys)
COSMIC
6g.49457756T>ACA364404079MMUTc.688A>T (p.Thr230Ser)
6g.49457756T>CCA364404082MMUTc.688A>G (p.Thr230Ala)
ClinVar dbSNP gnomAD v3 gnomAD v4
6g.49457756T>GCA364404085MMUTc.688A>C (p.Thr230Pro)
6g.49457756T=CA1627392094MMUTc.688A= (p.Thr230=)
6g.49457757A=CA1627392095MMUTc.687T= (p.Asn229=)
6g.49457757A>CCA364404089MMUTc.687T>G (p.Asn229Lys)
6g.49457757A>GCA3847069MMUTc.687T>C (p.Asn229=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
6g.49457757A>TCA364404104MMUTc.687T>A (p.Asn229Lys)
gnomAD v4
6g.49457758T>ACA364404107MMUTc.686A>T (p.Asn229Ile)
6g.49457758T>CCA364404110MMUTc.686A>G (p.Asn229Ser)
6g.49457758T>GCA364404113MMUTc.686A>C (p.Asn229Thr)
6g.49457759T>ACA364404116MMUTc.685A>T (p.Asn229Tyr)
6g.49457759T>CCA364404114MMUTc.685A>G (p.Asn229Asp)
6g.49457759T>GCA364404115MMUTc.685A>C (p.Asn229His)
6g.49457760T>ACA450608770MMUTc.684A>T (p.Arg228=)
6g.49457760T>CCA450608771MMUTc.684A>G (p.Arg228=)
6g.49457760T>GCA450608772MMUTc.684A>C (p.Arg228=)
6g.49457761C>ACA3847071MMUTc.683G>T (p.Arg228Leu)
dbSNP ExAC gnomAD v2
6g.49457761C=CA1627392096MMUTc.683G= (p.Arg228=)
6g.49457761C>GCA364404118MMUTc.683G>C (p.Arg228Pro)
6g.49457761C>TCA3847070MMUTc.683G>A (p.Arg228Gln)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
6g.49457762G>ACA312778MMUTc.682C>T (p.Arg228Ter)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
6g.49457762G>CCA364404123MMUTc.682C>G (p.Arg228Gly)
6g.49457762G=CA1627392097MMUTc.682C= (p.Arg228=)
6g.49457762G>TCA450608773MMUTc.682C>A (p.Arg228=)
6g.49457763A=CA1627392098MMUTc.681T= (p.Val227=)
6g.49457763A>CCA450608774MMUTc.681T>G (p.Val227=)
dbSNP gnomAD v2 gnomAD v4
6g.49457763A>GCA450608776MMUTc.681T>C (p.Val227=)
6g.49457763A>TCA450608775MMUTc.681T>A (p.Val227=)
6g.49457764A>CCA364404127MMUTc.680T>G (p.Val227Gly)
6g.49457764A>GCA364404129MMUTc.680T>C (p.Val227Ala)
6g.49457764A>TCA364404131MMUTc.680T>A (p.Val227Asp)
6g.49457765C>ACA364404135MMUTc.679G>T (p.Val227Phe)
6g.49457765C=CA1627392099MMUTc.679G= (p.Val227=)
6g.49457765C>GCA364404137MMUTc.679G>C (p.Val227Leu)
6g.49457765C>TCA364404139MMUTc.679G>A (p.Val227Ile)
6g.49457766dupCA913110644MMUTc.679dup (p.Val227GlyfsTer18)

Number of alleles fetched