Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
1 | g.173903978C>T | CA210746 | SERPINC1 | c.1306G>A (p.Ala436Thr) c.691G>A (p.Ala231Thr) c.1162G>A (p.Ala388Thr) c.1429G>A (p.Ala477Thr) c.1387G>A (p.Ala463Thr) c.1285G>A (p.Ala429Thr) c.1249G>A (p.Ala417Thr) c.1090G>A (p.Ala364Thr) | ClinVar dbSNP |
1 | g.173903978C= | CA1141581228 | SERPINC1 | c.1306G= (p.Ala436=) c.691G= (p.Ala231=) c.1162G= (p.Ala388=) c.1429G= (p.Ala477=) c.1387G= (p.Ala463=) c.1285G= (p.Ala429=) c.1249G= (p.Ala417=) c.1090G= (p.Ala364=) | dbSNP |