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. 2022 May 6;10(3):142–147. doi: 10.1016/j.prnil.2022.04.005

Table 2.

Prevalence of qualifying gene alterations.

Patients, n (%) Overall
Germline mutation
Somatic mutation
(n = 26) (n = 13) (n = 15)
BRCA2 13 (50) 11 (85) 2 (13)
CDK12 9 (35) 0 (0) 9 (60)
ATM 3 (12) 1 (8) 2 (13)
BRCA1 1 (4) 0 (0) 1 (7)
PALB2 1 (4) 0 (0) 1 (13)
RAD51D 1 (4) 1 (8) 0 (0)

Patients with multiple genes are included across more than one gene.

HRR: homologous recombination repair.