| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 5 | g.143295561T>A | CA126218 | NR3C1 | c.1922A>T (p.Asp641Val) c.1829A>T (p.Asp610Val) c.1925A>T (p.Asp642Val) c.1844A>T (p.Asp615Val) c.1667A>T (p.Asp556Val) c.1655A>T (p.Asp552Val) c.1631A>T (p.Asp544Val) c.977A>T (p.Asp326Val) c.932A>T (p.Asp311Val) c.917A>T (p.Asp306Val) c.731A>T (p.Asp244Val) n.845A>T | ClinVar dbSNP |
| 5 | g.143295561T= | CA3123355238 | NR3C1 | c.1922A= (p.Asp641=) c.1829A= (p.Asp610=) c.1925A= (p.Asp642=) c.1844A= (p.Asp615=) c.1667A= (p.Asp556=) c.1655A= (p.Asp552=) c.1631A= (p.Asp544=) c.977A= (p.Asp326=) c.932A= (p.Asp311=) c.917A= (p.Asp306=) c.731A= (p.Asp244=) n.845A= | dbSNP |