Total submissions: 1
| Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
|---|---|---|---|---|---|---|---|---|
| Gene |
RCV000160937 | SCV000211644 | pathogenic | Hereditary cancer-predisposing syndrome | 2014-10-09 | criteria provided, single submitter | clinical testing | This variant is denoted RAD51D c.270_271insTA (aka c.270_271dupTA) at the cDNA level and p.Lys91IlefsX13 (K91IfsX13) at the protein level. The normal sequence, with the bases that are duplicated in brackets, is TTGA{TA}AACT. The duplication causes a frameshift, which changes a Lysine to an Isoleucine at codon 91 in exon 4, and creates a premature stop codon at position 13 of the new reading frame. This mutation is predicted to cause loss of normal protein function through either protein truncation or nonsense-mediated mRNA decay. RAD51D 270_271dupTA has been observed in a woman with a history of both breast and ovarian cancer (Loveday 2011). We consider this mutation to be pathogenic.There have been multiple reports of a dominantly inherited predisposition to ovarian cancer due to pathogenic mutations in the RAD51D gene. Loveday et al. (2011) first reported this association in a cohort of 911 unrelated breast and ovarian cancer families in which 8 pathogenic mutations were identified. One of 1,060 controls was found to carry a mutation. Seven of the 8 mutations detected were identified in families with at least 2 cases of ovarian cancer. This study estimated that women with a RAD51D mutation have a 6.3-fold increased risk of ovarian cancer translating to a 9% lifetime risk. This study reports a small increased risk for breast cancer, but this was not statistically significant (Loveday 2011). Loveday et al. (2011) also showed that tumor cells with loss of function of RAD51D were sensitive to a clinical PARP inhibitor, and the effect was similar to cells with loss of function of the BRCA2 gene. Osher et al. (2012) reported the finding of one pathogenic RAD51D mutation in a series of 175 breast and ovarian cancer families. The proband in this family had ductal carcinoma in situ at age 47 and a significant family history of both breast and ovarian cancers (Osher 2012). The authors conclude that RAD51D mutations are primarily associated with ovarian cancer risk, but that there is a higher frequency of mutations in women with breast cancer who have a family history of ovarian cancer compared to breast cancer only families. This finding is supported in a recent study of 1,060 familial breast and/or ovarian cancer families, 741 of which were breast cancer only families, and 245 unselected ovarian cancer cases. Two deleterious RAD51D mutations were found in the unselected ovarian cancer group leading the authors to conclude that RAD51D mutations are very rare among familial breast cancer cases (Thompson 2013). The variant is found in HEREDICANCER panel(s). |