Chr Mutation (hg38) CAid Gene Transcript Linkouts
6g.49456141C>ACA3847025MMUTc.850G>T (p.Gly284Ter)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
6g.49456141C>TCA10575875MMUTc.850G>A (p.Gly284Arg)
 ClinVar dbSNP
6g.49456141C=CA1627391394MMUTc.850G= (p.Gly284=)
 dbSNP

Number of alleles fetched