| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 5 | g.143300556A>T | CA126225 | NR3C1 | c.1676T>A (p.Ile559Asn) c.1583T>A (p.Ile528Asn) c.1679T>A (p.Ile560Asn) c.1598T>A (p.Ile533Asn) c.1421T>A (p.Ile474Asn) c.1409T>A (p.Ile470Asn) c.1385T>A (p.Ile462Asn) c.731T>A (p.Ile244Asn) c.686T>A (p.Ile229Asn) c.671T>A (p.Ile224Asn) c.485T>A (p.Ile162Asn) n.599T>A | ClinVar dbSNP |
| 5 | g.143300556A= | CA3044572663 | NR3C1 | c.1676T= (p.Ile559=) c.1583T= (p.Ile528=) c.1679T= (p.Ile560=) c.1598T= (p.Ile533=) c.1421T= (p.Ile474=) c.1409T= (p.Ile470=) c.1385T= (p.Ile462=) c.731T= (p.Ile244=) c.686T= (p.Ile229=) c.671T= (p.Ile224=) c.485T= (p.Ile162=) n.599T= | dbSNP |