Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
X | g.139561902C>T | CA255405 | F9 | c.1217C>T (p.Ser406Leu) n.1723+161C>T c.1103C>T (p.Ser368Leu) c.1088C>T (p.Ser363Leu) | ClinVar dbSNP |
X | g.139561902C= | CA2461412230 | F9 | c.1217C= (p.Ser406=) n.1723+161C= c.1103C= (p.Ser368=) c.1088C= (p.Ser363=) | dbSNP |