Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
2 | g.127418286C>G | CA1286879830 | PROC | c.51C>G (p.Asp17Glu) | dbSNP |
2 | g.127418286C>T | CA11082294 | PROC | c.51C>T (p.Asp17=) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.127418286C= | CA1286879829 | PROC | c.51C= (p.Asp17=) | dbSNP |