Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
X | g.154903966G>A | CA255190 | F8 | c.5938C>T (p.His1980Tyr) c.5833C>T (p.His1945Tyr) | ClinVar dbSNP |
X | g.154903966G>C | CA414905825 | F8 | c.5938C>G (p.His1980Asp) c.5833C>G (p.His1945Asp) | dbSNP |
X | g.154903966G= | CA2466828154 | F8 | c.5938C= (p.His1980=) c.5833C= (p.His1945=) | dbSNP |