| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| X | g.154966664C>A | CA255036 | F8 | c.1033G>T (p.Val345Leu) c.*909G>T (n.*909G>T) c.928G>T (p.Val310Leu) | ClinVar dbSNP |
| X | g.154966664C>G | CA337336646 | F8 | c.1033G>C (p.Val345Leu) c.*909G>C (n.*909G>C) c.928G>C (p.Val310Leu) | dbSNP |
| X | g.154966664C= | CA2466848165 | F8 | c.1033G= (p.Val345=) c.*909G= (n.*909G=) c.928G= (p.Val310=) | dbSNP |