Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
X | g.154928647G>A | CA255155 | F8 | c.5143C>T (p.Arg1715Ter) c.5038C>T (p.Arg1680Ter) | ClinVar dbSNP COSMIC COSMIC |
X | g.154928647G>C | CA255157 | F8 | c.5143C>G (p.Arg1715Gly) c.5038C>G (p.Arg1680Gly) | ClinVar dbSNP |
X | g.154928647G>T | CA337327008 | F8 | c.5143C>A (p.Arg1715=) c.5038C>A (p.Arg1680=) | ClinVar dbSNP |