Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
X | g.154899876G>A | CA255200 | F8 | c.6263C>T (p.Ser2088Phe) c.6158C>T (p.Ser2053Phe) | ClinVar dbSNP |
X | g.154899876G>T | CA414902765 | F8 | c.6263C>A (p.Ser2088Tyr) c.6158C>A (p.Ser2053Tyr) | dbSNP |
X | g.154899876G= | CA2466827051 | F8 | c.6263C= (p.Ser2088=) c.6158C= (p.Ser2053=) | dbSNP |