| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| X | g.154966483A>G | CA414916092 | F8 | c.1214T>C (p.Ile405Thr) c.*1090T>C (n.*1090T>C) n.34T>C c.1109T>C (p.Ile370Thr) | dbSNP |
| X | g.154966483A>C | CA255098 | F8 | c.1214T>G (p.Ile405Ser) c.*1090T>G (n.*1090T>G) n.34T>G c.1109T>G (p.Ile370Ser) | ClinVar dbSNP |