Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
X | g.139561854T>A | CA414446295 | F9 | c.1169T>A (p.Ile390Asn) n.1723+113T>A c.1055T>A (p.Ile352Asn) c.1040T>A (p.Ile347Asn) | dbSNP |
X | g.139561854T>C | CA336143368 | F9 | c.1169T>C (p.Ile390Thr) n.1723+113T>C c.1055T>C (p.Ile352Thr) c.1040T>C (p.Ile347Thr) | dbSNP |