Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
X | g.154896102C>T | CA10567861 | F8 | c.6404G>A (p.Arg2135Gln) c.6299G>A (p.Arg2100Gln) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC |
X | g.154896102C>G | CA255029 | F8 | c.6404G>C (p.Arg2135Pro) c.6299G>C (p.Arg2100Pro) | ClinVar dbSNP |
X | g.154896102C= | CA2466826002 | F8 | c.6404G= (p.Arg2135=) c.6299G= (p.Arg2100=) | dbSNP |