| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 17 | g.61784355del | CA16620532 | BRIP1 | c.1036del (p.Glu346LysfsTer11) c.1543del (p.Glu515LysfsTer11) n.283del c.*969del (n.*969del) n.3284del c.1321del (p.Glu441LysfsTer11) c.147del c.1060del (p.Glu354LysfsTer11) c.1000del (p.Glu334LysfsTer11) | ClinVar dbSNP |
| 17 | g.61784355C= | CA3223488363 | BRIP1 | c.1036G= (p.Glu346=) c.1543G= (p.Glu515=) n.283G= c.*969G= (n.*969G=) n.3284G= c.1321G= (p.Glu441=) c.147G= c.1060G= (p.Glu354=) c.1000G= (p.Glu334=) | dbSNP dbSNP |