Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
11 | g.639830T>G | CA126864 | DRD4 | c.581T>G (p.Val194Gly) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.639830T>C | CA379007573 | DRD4 | c.581T>C (p.Val194Ala) | dbSNP |
11 | g.639830T= | CA1947226803 | DRD4 | c.581T= (p.Val194=) | dbSNP |
11 | g.639830T>A | CA379007572 | DRD4 | c.581T>A (p.Val194Asp) | dbSNP gnomAD v4 |