Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
X | g.154966525C>T | CA120918 | F8 | c.1172G>A (p.Arg391His) c.*1048G>A (n.*1048G>A) c.1067G>A (p.Arg356His) | ClinVar dbSNP COSMIC COSMIC |
X | g.154966525C>A | CA414916367 | F8 | c.1172G>T (p.Arg391Leu) c.*1048G>T (n.*1048G>T) c.1067G>T (p.Arg356Leu) | dbSNP |
X | g.154966525C= | CA2466848118 | F8 | c.1172G= (p.Arg391=) c.*1048G= (n.*1048G=) c.1067G= (p.Arg356=) | dbSNP |