| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 4 | g.154569648G>A | CA126431 | FGB | c.1093G>A (p.Ala365Thr) n.939+341G>A c.436G>A (p.Ala146Thr) c.916G>A (p.Ala306Thr) c.961G>A (p.Ala321Thr) c.793G>A (p.Ala265Thr) c.1084G>A (p.Ala362Thr) c.1080+13G>A (n.1080+13G>A) | ClinVar dbSNP |
| 4 | g.154569648G= | CA1504935402 | FGB | c.1093G= (p.Ala365=) n.939+341G= c.436G= (p.Ala146=) c.916G= (p.Ala306=) c.961G= (p.Ala321=) c.793G= (p.Ala265=) c.1084G= (p.Ala362=) c.1080+13G= (n.1080+13G=) | dbSNP |