| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 13 | g.32371100G>A | CA025745 | BRCA2 | c.8632G>A (p.Glu2878Lys) c.8632G>A (p.Val2878Ile) c.8263G>A (p.Glu2755Lys) c.1099G>A (p.Glu367Lys) c.8640G>A (n.8640G>A) c.1197G>A c.130G>A (p.Val44Ile) c.8536G>A (p.Glu2846Lys) | ClinVar dbSNP |
| 13 | g.32371100G>C | CA387753025 | BRCA2 | c.8632G>C (p.Glu2878Gln) c.8632G>C (p.Val2878Leu) c.8263G>C (p.Glu2755Gln) c.1099G>C (p.Glu367Gln) c.8640G>C (n.8640G>C) c.1197G>C c.130G>C (p.Val44Leu) c.8536G>C (p.Glu2846Gln) | ClinVar dbSNP |
| 13 | g.32371100G= | CA2082816587 | BRCA2 | c.8632G= (p.Glu2878=) c.8632G= (p.Val2878=) c.8263G= (p.Glu2755=) c.1099G= (p.Glu367=) c.8640G= (n.8640G=) c.1197G= c.130G= (p.Val44=) c.8536G= (p.Glu2846=) | dbSNP |