| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 13 | g.32362593T>A | CA16614217 | BRCA2 | c.7876T>A (p.Trp2626Arg) c.7507T>A (p.Trp2503Arg) c.343T>A (p.Trp115Arg) c.7884T>A (p.Asp2628Glu) c.441T>A n.7884T>A c.7780T>A (p.Trp2594Arg) | ClinVar dbSNP |
| 13 | g.32362593T>C | CA387747100 | BRCA2 | c.7876T>C (p.Trp2626Arg) c.7507T>C (p.Trp2503Arg) c.343T>C (p.Trp115Arg) c.7884T>C (p.Asp2628=) c.441T>C n.7884T>C c.7780T>C (p.Trp2594Arg) | ClinVar dbSNP |
| 13 | g.32362593T= | CA2082831005 | BRCA2 | c.7876T= (p.Trp2626=) c.7507T= (p.Trp2503=) c.343T= (p.Trp115=) c.7884T= (p.Asp2628=) c.441T= n.7884T= c.7780T= (p.Trp2594=) | dbSNP |
| 13 | g.32362593T>G | CA387747101 | BRCA2 | c.7876T>G (p.Trp2626Gly) c.7507T>G (p.Trp2503Gly) c.343T>G (p.Trp115Gly) c.7884T>G (p.Asp2628Glu) c.441T>G n.7884T>G c.7780T>G (p.Trp2594Gly) | dbSNP gnomAD v4 |