| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 13 | g.32376767del | CA025795 | BRCA2 | c.8730del (p.Asn2910LysfsTer17) c.*97del (n.*97del) c.8361del (p.Asn2787LysfsTer17) c.*292del (n.*292del) c.1197del (p.Asn399LysfsTer17) n.857del c.8738del (n.8738del) c.1608del c.292del (n.292del) c.8634del (p.Asn2878LysfsTer17) c.8730del (p.Asn2910LysfsTer?) | ClinVar dbSNP |
| 13 | g.32376767T= | CA2082829367 | BRCA2 | c.8730T= (p.Asn2910=) c.*97T= (n.*97T=) c.8361T= (p.Asn2787=) c.*292T= (n.*292T=) c.1197T= (p.Asn399=) n.857T= c.8738T= (n.8738T=) c.1608T= c.292T= (n.292T=) c.8634T= (p.Asn2878=) | dbSNP dbSNP |