| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| X | g.154947782A>G | CA255136 | F8 | c.2029T>C (p.Phe677Leu) c.*1779+6110T>C (n.*1779+6110T>C) c.1924T>C (p.Phe642Leu) | ClinVar dbSNP |
| X | g.154947782A= | CA2466842539 | F8 | c.2029T= (p.Phe677=) c.*1779+6110T= (n.*1779+6110T=) c.1924T= (p.Phe642=) | dbSNP |