| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 5 | g.143300520A>G | CA126229 | NR3C1 | c.1712T>C (p.Val571Ala) c.1619T>C (p.Val540Ala) c.1715T>C (p.Val572Ala) c.1634T>C (p.Val545Ala) c.1457T>C (p.Val486Ala) c.1445T>C (p.Val482Ala) c.1421T>C (p.Val474Ala) c.767T>C (p.Val256Ala) c.722T>C (p.Val241Ala) c.707T>C (p.Val236Ala) c.521T>C (p.Val174Ala) n.635T>C | ClinVar dbSNP |
| 5 | g.143300520A= | CA2581508697 | NR3C1 | c.1712T= (p.Val571=) c.1619T= (p.Val540=) c.1715T= (p.Val572=) c.1634T= (p.Val545=) c.1457T= (p.Val486=) c.1445T= (p.Val482=) c.1421T= (p.Val474=) c.767T= (p.Val256=) c.722T= (p.Val241=) c.707T= (p.Val236=) c.521T= (p.Val174=) n.635T= | dbSNP |