Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
X | g.154896103G>A | CA255011 | F8 | c.6403C>T (p.Arg2135Ter) c.6298C>T (p.Arg2100Ter) | ClinVar dbSNP COSMIC COSMIC |
X | g.154896103G>C | CA414899439 | F8 | c.6403C>G (p.Arg2135Gly) c.6298C>G (p.Arg2100Gly) | dbSNP |
X | g.154896103G>T | CA519352452 | F8 | c.6403C>A (p.Arg2135=) c.6298C>A (p.Arg2100=) | dbSNP gnomAD v4 |