| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| X | g.154987242T>C | CA414919205 | F8 | c.665A>G (p.Asp222Gly) c.*451A>G (n.*451A>G) c.560A>G (p.Asp187Gly) | dbSNP |
| X | g.154987242T>G | CA414919206 | F8 | c.665A>C (p.Asp222Ala) c.*451A>C (n.*451A>C) c.560A>C (p.Asp187Ala) | ClinVar dbSNP |
| X | g.154987242T>A | CA255068 | F8 | c.665A>T (p.Asp222Val) c.*451A>T (n.*451A>T) c.560A>T (p.Asp187Val) | ClinVar dbSNP |