| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| X | g.139541126G>T | CA414437535 | F9 | c.328G>T (p.Asp110Tyr) c.277+3740G>T (n.277+3740G>T) n.281G>T | dbSNP |
| X | g.139541126G>A | CA255435 | F9 | c.328G>A (p.Asp110Asn) c.277+3740G>A (n.277+3740G>A) n.281G>A | ClinVar dbSNP COSMIC |
| X | g.139541126G= | CA2461405479 | F9 | c.328G= (p.Asp110=) c.277+3740G= (n.277+3740G=) n.281G= | dbSNP |