Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
2 | g.127418299G>C | CA1286879837 | PROC | c.64G>C (p.Gly22Arg) | dbSNP |
2 | g.127418299G>T | CA1286879836 | PROC | c.64G>T (p.Gly22Trp) | dbSNP gnomAD v4 |
2 | g.127418299G>A | CA11233235 | PROC | c.64G>A (p.Gly22Arg) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |