Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
13 | g.32363407_32363408del | CA025511 | BRCA2 | c.8205_8206del (p.Leu2737SerfsTer26) c.7836_7837del (p.Leu2614SerfsTer26) c.672_673del (p.Leu226SerfsTer26) c.8213_8214del (n.8213_8214del) c.770_771del c.8109_8110del (p.Leu2705SerfsTer26) | ClinVar dbSNP |
13 | g.32363408dup | CA025513 | BRCA2 | c.8206dup (p.Leu2736ProfsTer28) c.7837dup (p.Leu2613ProfsTer28) c.673dup (p.Leu225ProfsTer28) c.8214dup (n.8214dup) c.771dup c.8110dup (p.Leu2704ProfsTer28) | ClinVar dbSNP ExAC |
13 | g.32363408del | CA645509333 | BRCA2 | c.8206del (p.Leu2736SerfsTer2) c.7837del (p.Leu2613SerfsTer2) c.673del (p.Leu225SerfsTer2) c.8214del (n.8214del) c.771del c.8110del (p.Leu2704SerfsTer2) | ClinVar dbSNP |