| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| X | g.139562042T>C | CA255422 | F9 | c.1357T>C (p.Trp453Arg) n.1723+301T>C c.1243T>C (p.Trp415Arg) c.1228T>C (p.Trp410Arg) | ClinVar dbSNP |
| X | g.139562042T= | CA2461412305 | F9 | c.1357T= (p.Trp453=) n.1723+301T= c.1243T= (p.Trp415=) c.1228T= (p.Trp410=) | dbSNP |