| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| X | g.154904493G>C | CA255178 | F8 | c.5618C>G (p.Pro1873Arg) c.5513C>G (p.Pro1838Arg) | ClinVar dbSNP |
| X | g.154904493G>A | CA414908172 | F8 | c.5618C>T (p.Pro1873Leu) c.5513C>T (p.Pro1838Leu) | dbSNP gnomAD v3 gnomAD v4 |
| X | g.154904493G= | CA2466828317 | F8 | c.5618C= (p.Pro1873=) c.5513C= (p.Pro1838=) | dbSNP |