Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
X | g.139541076A>G | CA255322 | F9 | c.278A>G (p.Asp93Gly) c.277+3690A>G (n.277+3690A>G) n.242-11A>G | ClinVar dbSNP |
X | g.139541076A>T | CA414437358 | F9 | c.278A>T (p.Asp93Val) c.277+3690A>T (n.277+3690A>T) n.242-11A>T | dbSNP |
X | g.139541076A= | CA2461405465 | F9 | c.278A= (p.Asp93=) c.277+3690A= (n.277+3690A=) n.242-11A= | dbSNP |