Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
X | g.139561916A>G | CA255441 | F9 | c.1231A>G (p.Ser411Gly) n.1723+175A>G c.1117A>G (p.Ser373Gly) c.1102A>G (p.Ser368Gly) | ClinVar dbSNP |
X | g.139561916A= | CA2461412241 | F9 | c.1231A= (p.Ser411=) n.1723+175A= c.1117A= (p.Ser373=) c.1102A= (p.Ser368=) | dbSNP |