Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
7 | g.122995119A>G | CA457464841 | TAS2R16 | c.516T>C (p.Asn172=) | dbSNP |
7 | g.122995119A>C | CA117409 | TAS2R16 | c.516T>G (p.Asn172Lys) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.122995119A>T | CA369149190 | TAS2R16 | c.516T>A (p.Asn172Lys) | dbSNP |
7 | g.122995119A= | CA1739876990 | TAS2R16 | c.516T= (p.Asn172=) | dbSNP |