Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
X | g.139561710C>T | CA255381 | F9 | c.1025C>T (p.Thr342Met) n.1692C>T c.911C>T (p.Thr304Met) c.896C>T (p.Thr299Met) | ClinVar dbSNP gnomAD v4 COSMIC |
X | g.139561710C>G | CA414445449 | F9 | c.1025C>G (p.Thr342Arg) n.1692C>G c.911C>G (p.Thr304Arg) c.896C>G (p.Thr299Arg) | dbSNP |
X | g.139561710C>A | CA414445446 | F9 | c.1025C>A (p.Thr342Lys) n.1692C>A c.911C>A (p.Thr304Lys) c.896C>A (p.Thr299Lys) | dbSNP |