| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 2 | g.127426227G>C | CA114416 | PROC | c.678G>C (p.Gln226His) c.121-2130G>C c.780G>C (p.Gln260His) n.264G>C c.861G>C (p.Gln287His) c.843G>C (p.Gln281His) c.741G>C (p.Gln247His) c.921G>C (p.Gln307His) c.1023G>C (p.Gln341His) c.963G>C (p.Gln321His) n.4358C>G c.846G>C (p.Gln282His) c.864G>C (p.Gln288His) c.621G>C (p.Gln207His) c.654G>C (p.Gln218His) c.672G>C (p.Gln224His) | ClinVar dbSNP |
| 2 | g.127426227G>A | CA428618368 | PROC | c.678G>A (p.Gln226=) c.121-2130G>A c.780G>A (p.Gln260=) n.264G>A c.861G>A (p.Gln287=) c.843G>A (p.Gln281=) c.741G>A (p.Gln247=) c.921G>A (p.Gln307=) c.1023G>A (p.Gln341=) c.963G>A (p.Gln321=) n.4358C>T c.846G>A (p.Gln282=) c.864G>A (p.Gln288=) c.621G>A (p.Gln207=) c.654G>A (p.Gln218=) c.672G>A (p.Gln224=) | ClinVar dbSNP gnomAD v2 gnomAD v4 |