Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
X | g.139541127A>G | CA255331 | F9 | c.329A>G (p.Asp110Gly) c.277+3741A>G (n.277+3741A>G) n.282A>G | ClinVar dbSNP |
X | g.139541127A>T | CA414437538 | F9 | c.329A>T (p.Asp110Val) c.277+3741A>T (n.277+3741A>T) n.282A>T | dbSNP |
X | g.139541127A= | CA2461405480 | F9 | c.329A= (p.Asp110=) c.277+3741A= (n.277+3741A=) n.282A= | dbSNP |