Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
X | g.154904025C>T | CA255019 | F8 | c.5879G>A (p.Arg1960Gln) c.5774G>A (p.Arg1925Gln) | ClinVar dbSNP |
X | g.154904025C>A | CA255185 | F8 | c.5879G>T (p.Arg1960Leu) c.5774G>T (p.Arg1925Leu) | ClinVar dbSNP |
X | g.154904025C= | CA2466828175 | F8 | c.5879G= (p.Arg1960=) c.5774G= (p.Arg1925=) | dbSNP |