| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| X | g.139561911G>T | CA336143415 | F9 | c.1226G>T (p.Gly409Val) n.1723+170G>T c.1112G>T (p.Gly371Val) c.1097G>T (p.Gly366Val) | dbSNP |
| X | g.139561911G>C | CA414446616 | F9 | c.1226G>C (p.Gly409Ala) n.1723+170G>C c.1112G>C (p.Gly371Ala) c.1097G>C (p.Gly366Ala) | dbSNP |