Chr Mutation (hg38) CAid Gene Transcript Linkouts
6g.49451517_49451518delinsTACA2580074725MMUTc.1280_1281delinsTA (p.Gly427Val)
ClinVar
6g.49451518C>ACA364398737MMUTc.1280G>T (p.Gly427Val)
6g.49451518C=CA1627389301MMUTc.1280G= (p.Gly427=)
6g.49451518C>GCA364398738MMUTc.1280G>C (p.Gly427Ala)
6g.49451518C>TCA347873MMUTc.1280G>A (p.Gly427Asp)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
6g.49451519C>ACA364398739MMUTc.1279G>T (p.Gly427Cys)
6g.49451519C=CA1627389302MMUTc.1279G= (p.Gly427=)
6g.49451519C>GCA364398740MMUTc.1279G>C (p.Gly427Arg)
6g.49451519C>TCA364398741MMUTc.1279G>A (p.Gly427Ser)
ClinVar dbSNP gnomAD v2 gnomAD v4
6g.49451520T>ACA3846927MMUTc.1278A>T (p.Gly426=)
dbSNP ExAC gnomAD v2 gnomAD v4
6g.49451520T>CCA450606216MMUTc.1278A>G (p.Gly426=)
6g.49451520T>GCA450606217MMUTc.1278A>C (p.Gly426=)
6g.49451520T=CA1627389303MMUTc.1278A= (p.Gly426=)
6g.49451521C>ACA364398742MMUTc.1277G>T (p.Gly426Val)
gnomAD v4
6g.49451521C=CA1627389304MMUTc.1277G= (p.Gly426=)
6g.49451521C>GCA138796331MMUTc.1277G>C (p.Gly426Ala)
dbSNP gnomAD v3 gnomAD v4
6g.49451521C>TCA10575866MMUTc.1277G>A (p.Gly426Glu)
ClinVar dbSNP
6g.49451522C>ACA364398743MMUTc.1276G>T (p.Gly426Ter)
6g.49451522C=CA1627389305MMUTc.1276G= (p.Gly426=)
6g.49451522C>GCA364398744MMUTc.1276G>C (p.Gly426Arg)
6g.49451522C>TCA138796335MMUTc.1276G>A (p.Gly426Arg)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
6g.49451523C>ACA364398745MMUTc.1275G>T (p.Trp425Cys)
6g.49451523C>GCA364398746MMUTc.1275G>C (p.Trp425Cys)
6g.49451523C>TCA364398747MMUTc.1275G>A (p.Trp425Ter)
6g.49451524C>ACA364398748MMUTc.1274G>T (p.Trp425Leu)
6g.49451524C>GCA364398749MMUTc.1274G>C (p.Trp425Ser)
6g.49451524C>TCA364398750MMUTc.1274G>A (p.Trp425Ter)
ClinVar dbSNP gnomAD v4
6g.49451525A>CCA364398752MMUTc.1273T>G (p.Trp425Gly)
6g.49451525A>GCA364398753MMUTc.1273T>C (p.Trp425Arg)
6g.49451525A>TCA364398751MMUTc.1273T>A (p.Trp425Arg)
6g.49451526A>CCA450606242MMUTc.1272T>G (p.Pro424=)
6g.49451526A>GCA450606240MMUTc.1272T>C (p.Pro424=)
ClinVar dbSNP gnomAD v4
6g.49451526A>TCA450606239MMUTc.1272T>A (p.Pro424=)
6g.49451527G>ACA10575867MMUTc.1271C>T (p.Pro424Leu)
ClinVar dbSNP
6g.49451527G>CCA364398754MMUTc.1271C>G (p.Pro424Arg)
6g.49451527G=CA1627389306MMUTc.1271C= (p.Pro424=)
6g.49451527G>TCA364398755MMUTc.1271C>A (p.Pro424His)
6g.49451528delCA2679046690MMUTc.1271del (p.Pro424LeufsTer7)
gnomAD v4
6g.49451528G>ACA3846928MMUTc.1270C>T (p.Pro424Ser)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
6g.49451528G>CCA364398756MMUTc.1270C>G (p.Pro424Ala)
dbSNP gnomAD v4
6g.49451528G=CA1627389307MMUTc.1270C= (p.Pro424=)
6g.49451528G>TCA364398757MMUTc.1270C>A (p.Pro424Thr)
gnomAD v4
6g.49451529A>CCA364398759MMUTc.1269T>G (p.Asp423Glu)
6g.49451529A>GCA450606251MMUTc.1269T>C (p.Asp423=)
6g.49451529A>TCA364398758MMUTc.1269T>A (p.Asp423Glu)
6g.49451530T>ACA364398760MMUTc.1268A>T (p.Asp423Val)
6g.49451530T>CCA364398761MMUTc.1268A>G (p.Asp423Gly)
dbSNP
6g.49451530T>GCA364398762MMUTc.1268A>C (p.Asp423Ala)
6g.49451530T=CA1627389308MMUTc.1268A= (p.Asp423=)
6g.49451531C>ACA364398763MMUTc.1267G>T (p.Asp423Tyr)

Number of alleles fetched