Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
3 | g.98007903A>G | CA79557112 | GABRR3 | c.615T>C (p.Tyr205=) n.501+4441T>C | dbSNP gnomAD v4 |
3 | g.98007903A>T | CA79557113 | GABRR3 | c.615T>A (p.Tyr205Ter) n.501+4441T>A | ClinVar dbSNP gnomAD v3 gnomAD v4 |
3 | g.98007903A>C | CA353597894 | GABRR3 | c.615T>G (p.Tyr205Ter) n.501+4441T>G | dbSNP |