Chr Mutation (hg38) CAid Gene Transcript Linkouts
1g.97082391T>ACA228077DPYDc.2846A>T (p.Asp949Val)
c.2630A>T (p.Asp877Val)
c.2735A>T (p.Asp912Val)
c.2351A>T (p.Asp784Val)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
1g.97082391T=CA1140768466DPYDc.2846A= (p.Asp949=)
c.2630A= (p.Asp877=)
c.2735A= (p.Asp912=)
c.2351A= (p.Asp784=)
dbSNP

Number of alleles fetched