| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| X | g.154904518C>A | CA255176 | F8 | c.5593G>T (p.Asp1865Tyr) c.5488G>T (p.Asp1830Tyr) | ClinVar dbSNP COSMIC COSMIC |
| X | g.154904518C>T | CA255175 | F8 | c.5593G>A (p.Asp1865Asn) c.5488G>A (p.Asp1830Asn) | ClinVar dbSNP |
| X | g.154904518C= | CA2466828329 | F8 | c.5593G= (p.Asp1865=) c.5488G= (p.Asp1830=) | dbSNP |