| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| X | g.154863112C>A | CA414907082 | F8 | c.6545G>T (p.Arg2182Leu) c.278G>T (p.Arg93Leu) c.140G>T (p.Arg47Leu) c.6440G>T (p.Arg2147Leu) | dbSNP |
| X | g.154863112C>T | CA255213 | F8 | c.6545G>A (p.Arg2182His) c.278G>A (p.Arg93His) c.140G>A (p.Arg47His) c.6440G>A (p.Arg2147His) | ClinVar dbSNP COSMIC COSMIC |