Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
6 | g.125928768T>G | CA3987382 | NCOA7 | c.2826T>G (p.Asp942Glu) c.2481T>G (p.Asp827Glu) c.657T>G (p.Asp219Glu) c.*103T>G (n.*103T>G) c.2793T>G (p.Asp931Glu) n.3073T>G | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
6 | g.125928768T>C | CA451994810 | NCOA7 | c.2826T>C (p.Asp942=) c.2481T>C (p.Asp827=) c.657T>C (p.Asp219=) c.*103T>C (n.*103T>C) c.2793T>C (p.Asp931=) n.3073T>C | dbSNP gnomAD v4 |