Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
X | g.154903951G>A | CA255191 | F8 | c.5953C>T (p.Arg1985Ter) c.5848C>T (p.Arg1950Ter) | ClinVar dbSNP COSMIC COSMIC |
X | g.154903951G>C | CA414905720 | F8 | c.5953C>G (p.Arg1985Gly) c.5848C>G (p.Arg1950Gly) | ClinVar dbSNP |
X | g.154903951G= | CA2466828148 | F8 | c.5953C= (p.Arg1985=) c.5848C= (p.Arg1950=) | dbSNP |