Chr Mutation (hg38) CAid Gene Transcript Linkouts
6g.49459189C>ACA364405090MMUTc.278G>T (p.Arg93Leu)
6g.49459189C=CA1627396731MMUTc.278G= (p.Arg93=)
6g.49459189C>GCA364405091MMUTc.278G>C (p.Arg93Pro)
6g.49459189C>TCA249728MMUTc.278G>A (p.Arg93His)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
6g.49459190G>ACA3847146MMUTc.277C>T (p.Arg93Cys)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
6g.49459190G>CCA364405092MMUTc.277C>G (p.Arg93Gly)
6g.49459190G=CA1627396737MMUTc.277C= (p.Arg93=)
6g.49459190G>TCA364405093MMUTc.277C>A (p.Arg93Ser)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
6g.49459191T>ACA450609577MMUTc.276A>T (p.Thr92=)
6g.49459191T>CCA450609578MMUTc.276A>G (p.Thr92=)
COSMIC
6g.49459191T>GCA450609580MMUTc.276A>C (p.Thr92=)
6g.49459192G>ACA364405094MMUTc.275C>T (p.Thr92Ile)
6g.49459192G>CCA364405096MMUTc.275C>G (p.Thr92Arg)
6g.49459192G>TCA364405097MMUTc.275C>A (p.Thr92Lys)
6g.49459193T>ACA364405098MMUTc.274A>T (p.Thr92Ser)
6g.49459193T>CCA364405099MMUTc.274A>G (p.Thr92Ala)
dbSNP
6g.49459193T>GCA364405101MMUTc.274A>C (p.Thr92Pro)
6g.49459193T=CA1627396743MMUTc.274A= (p.Thr92=)
6g.49459194G>ACA450609584MMUTc.273C>T (p.Phe91=)
dbSNP
6g.49459194G>CCA364405107MMUTc.273C>G (p.Phe91Leu)
6g.49459194G=CA1627396747MMUTc.273C= (p.Phe91=)
6g.49459194G>TCA364405105MMUTc.273C>A (p.Phe91Leu)
6g.49459195A>CCA364405109MMUTc.272T>G (p.Phe91Cys)
6g.49459195A>GCA364405110MMUTc.272T>C (p.Phe91Ser)
6g.49459195A>TCA364405112MMUTc.272T>A (p.Phe91Tyr)
6g.49459196A>CCA364405115MMUTc.271T>G (p.Phe91Val)
6g.49459196A>GCA364405116MMUTc.271T>C (p.Phe91Leu)
6g.49459196A>TCA364405117MMUTc.271T>A (p.Phe91Ile)
6g.49459197T>ACA450609593MMUTc.270A>T (p.Pro90=)
6g.49459197T>CCA450609591MMUTc.270A>G (p.Pro90=)
6g.49459197T>GCA450609592MMUTc.270A>C (p.Pro90=)
6g.49459198G>ACA364405119MMUTc.269C>T (p.Pro90Leu)
gnomAD v4
6g.49459198G>CCA364405121MMUTc.269C>G (p.Pro90Arg)
6g.49459198G=CA1627396750MMUTc.269C= (p.Pro90=)
6g.49459198G>TCA364405122MMUTc.269C>A (p.Pro90Gln)
dbSNP
6g.49459199G>ACA364405127MMUTc.268C>T (p.Pro90Ser)
6g.49459199G>CCA364405129MMUTc.268C>G (p.Pro90Ala)
6g.49459199G>TCA364405131MMUTc.268C>A (p.Pro90Thr)
6g.49459199delinsTTCA2695206698MMUTc.268delinsAA (p.Pro90AsnfsTer14)
6g.49459200C>ACA364405133MMUTc.267G>T (p.Lys89Asn)
6g.49459200C=CA1627396754MMUTc.267G= (p.Lys89=)
6g.49459200C>GCA364405132MMUTc.267G>C (p.Lys89Asn)
6g.49459200C>TCA450609595MMUTc.267G>A (p.Lys89=)
ClinVar dbSNP gnomAD v4
6g.49459201T>ACA364405134MMUTc.266A>T (p.Lys89Met)
6g.49459201T>CCA364405135MMUTc.266A>G (p.Lys89Arg)
6g.49459201T>GCA364405136MMUTc.266A>C (p.Lys89Thr)
COSMIC
6g.49459202T>ACA364405138MMUTc.265A>T (p.Lys89Ter)
6g.49459202T>CCA364405139MMUTc.265A>G (p.Lys89Glu)
6g.49459202T>GCA364405141MMUTc.265A>C (p.Lys89Gln)
6g.49459203C>ACA450609600MMUTc.264G>T (p.Val88=)

Number of alleles fetched