Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
X | g.154863113G>A | CA255214 | F8 | c.6544C>T (p.Arg2182Cys) c.277C>T (p.Arg93Cys) c.139C>T (p.Arg47Cys) c.6439C>T (p.Arg2147Cys) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC |
X | g.154863113G= | CA2466815607 | F8 | c.6544C= (p.Arg2182=) c.277C= (p.Arg93=) c.139C= (p.Arg47=) c.6439C= (p.Arg2147=) | dbSNP |