| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 1 | g.173904013C>T | CA210785 | SERPINC1 | c.1271G>A (p.Gly424Asp) c.656G>A (p.Gly219Asp) c.1127G>A (p.Gly376Asp) c.1394G>A (p.Gly465Asp) c.1352G>A (p.Gly451Asp) c.1250G>A (p.Gly417Asp) c.1214G>A (p.Gly405Asp) c.1055G>A (p.Gly352Asp) | ClinVar dbSNP |
| 1 | g.173904013C= | CA1141581237 | SERPINC1 | c.1271G= (p.Gly424=) c.656G= (p.Gly219=) c.1127G= (p.Gly376=) c.1394G= (p.Gly465=) c.1352G= (p.Gly451=) c.1250G= (p.Gly417=) c.1214G= (p.Gly405=) c.1055G= (p.Gly352=) | dbSNP |