Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
16 | g.31094624C>T | CA395732750 | VKORC1 | c.106G>A (p.Asp36Asn) c.245+765G>A c.270+765G>A (n.270+765G>A) n.894G>A | dbSNP gnomAD v2 gnomAD v4 |
16 | g.31094624C>A | CA115418 | VKORC1 | c.106G>T (p.Asp36Tyr) c.245+765G>T c.270+765G>T (n.270+765G>T) n.894G>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |