Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
4 | g.148081384T>G | CA358425248 | NR3C2 | c.2915A>C (p.Glu972Ala) c.*298A>C (n.*298A>C) c.2927A>C (p.Glu976Ala) c.2564A>C (p.Glu855Ala) n.2782A>C n.2676A>C | dbSNP |
4 | g.148081384T>C | CA119757 | NR3C2 | c.2915A>G (p.Glu972Gly) c.*298A>G (n.*298A>G) c.2927A>G (p.Glu976Gly) c.2564A>G (p.Glu855Gly) n.2782A>G n.2676A>G | ClinVar dbSNP |