Chr Mutation (hg38) CAid Gene Transcript Linkouts
6g.144187018C>TCA275513STX11c.391C>T (p.Gln131Ter)
c.469C>T (p.Gln157Ter)
ClinVar dbSNP gnomAD v4
6g.144187018C=CA1669582624STX11c.391C= (p.Gln131=)
c.469C= (p.Gln157=)
dbSNP

Number of alleles fetched