Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
11 | g.59443715G>C | CA380775040 | OR5A1 | c.547G>C (p.Asp183His) | dbSNP |
11 | g.59443715G>T | CA380775045 | OR5A1 | c.547G>T (p.Asp183Tyr) | dbSNP |
11 | g.59443715G>A | CA6018375 | OR5A1 | c.547G>A (p.Asp183Asn) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.59443715G= | CA1976399065 | OR5A1 | c.547G= (p.Asp183=) | dbSNP |