| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| X | g.139561913G>C | CA255443 | F9 | c.1228G>C (p.Asp410His) n.1723+172G>C c.1114G>C (p.Asp372His) c.1099G>C (p.Asp367His) | ClinVar dbSNP |
| X | g.139561913G= | CA2461412239 | F9 | c.1228G= (p.Asp410=) n.1723+172G= c.1114G= (p.Asp372=) c.1099G= (p.Asp367=) | dbSNP |