| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 5 | g.143281964T>A | CA126221 | NR3C1 | c.2259A>T (p.Leu753Phe) c.2166A>T (p.Leu722Phe) c.2262A>T (p.Leu754Phe) c.2181+604A>T (n.2181+604A>T) c.2181A>T (p.Leu727Phe) c.2004A>T (p.Leu668Phe) c.1992A>T (p.Leu664Phe) c.1968A>T (p.Leu656Phe) c.1314A>T (p.Leu438Phe) c.1269A>T (p.Leu423Phe) c.1254A>T (p.Leu418Phe) c.1068A>T (p.Leu356Phe) n.656-2735T>A n.1182A>T | ClinVar dbSNP COSMIC |
| 5 | g.143281964T= | CA2581520110 | NR3C1 | c.2259A= (p.Leu753=) c.2166A= (p.Leu722=) c.2262A= (p.Leu754=) c.2181+604A= (n.2181+604A=) c.2181A= (p.Leu727=) c.2004A= (p.Leu668=) c.1992A= (p.Leu664=) c.1968A= (p.Leu656=) c.1314A= (p.Leu438=) c.1269A= (p.Leu423=) c.1254A= (p.Leu418=) c.1068A= (p.Leu356=) n.656-2735T= n.1182A= | dbSNP |