| | | Deletion (genic downstream transcript variant) | Uterine corpus cancer | |
| | | Duplication (frameshift variant) | Endometrial carcinoma | |
| | | Deletion (frameshift variant) | Endometrial carcinoma | |
| | | Single nucleotide variant (nonsense) | Endometrial carcinoma | |
| | | Deletion (splice donor variant) | Hepatocellular carcinoma | |
| | | Deletion (frameshift variant) | Hepatocellular carcinoma | |
| | | Deletion (splice acceptor variant +1 more) | Hepatocellular carcinoma | |
| | | Single nucleotide variant (splice acceptor variant) | Carcinoma of pancreas | |
| | | Duplication (frameshift variant) | Carcinoma of pancreas | |
| | | Deletion (splice acceptor variant +1 more) | TUMOR PREDISPOSITION SYNDROME 4, BREAST/PROSTATE +2 more | |
| | | Deletion (frameshift variant) | Carcinoma of pancreas | |
| | | Deletion (frameshift variant +1 more) | Carcinoma of pancreas | |
| | | Deletion (frameshift variant) | Breast and/or ovarian cancer | |
| | | Duplication (frameshift variant) | Hereditary cancer-predisposing syndrome | |
| | RAD51D, RAD51L3-RFFL (C182fs +2 more) | Deletion (non-coding transcript variant +1 more) | Hereditary cancer-predisposing syndrome | |
| | RAD51D, RAD51L3-RFFL (Q192* +2 more) | Single nucleotide variant (non-coding transcript variant +1 more) | Hereditary cancer-predisposing syndrome | |
| | | Deletion (frameshift variant) | Breast and/or ovarian cancer | |
| | | Deletion (frameshift variant +1 more) | Breast and/or ovarian cancer | |
| | LOC129390903, RAD51C (Q222*) | Single nucleotide variant (nonsense +1 more) | Breast and/or ovarian cancer | |
| | | Deletion (frameshift variant) | Hereditary cancer-predisposing syndrome | |
| | | Deletion (frameshift variant) | Breast and/or ovarian cancer | |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | Microcephaly, normal intelligence and immunodeficiency | |
| | | Deletion | Breast and/or ovarian cancer | |
| | | Deletion | Breast and/or ovarian cancer | |
| | | Deletion | Breast and/or ovarian cancer | |
| | | Deletion (frameshift variant +1 more) | Breast and/or ovarian cancer | |
| | | Indel (splice acceptor variant +2 more) | Breast and/or ovarian cancer | |
| | | Indel (splice acceptor variant +2 more) | Breast and/or ovarian cancer | |
| | | Deletion (splice acceptor variant +1 more) | Breast and/or ovarian cancer | |
| | | Duplication (frameshift variant +1 more) | Breast and/or ovarian cancer | |
| | | Single nucleotide variant (nonsense) | Microcephaly, normal intelligence and immunodeficiency | |
| | | Indel (splice acceptor variant +1 more) | Breast and/or ovarian cancer | |
| | | Duplication (splice donor variant +1 more) | Breast and/or ovarian cancer | |
| | | Microsatellite (frameshift variant +1 more) | Hereditary cancer-predisposing syndrome +1 more | |
| | | Duplication (frameshift variant) | Breast and/or ovarian cancer | |
| | | Insertion (frameshift variant +1 more) | Hereditary cancer-predisposing syndrome +2 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (nonsense) | Microcephaly, normal intelligence and immunodeficiency +2 more | |
| | | Single nucleotide variant (splice donor variant) | Hereditary cancer-predisposing syndrome | |
| | | Microsatellite (frameshift variant) | Hereditary nonpolyposis colorectal neoplasms +3 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (nonsense) | Familial cancer of breast +1 more | |
| | | Duplication (frameshift variant) | Fanconi anemia complementation group E +1 more | GPathogenic/Likely pathogenic |
| | | Duplication (frameshift variant +1 more) | Hereditary cancer-predisposing syndrome +2 more | |
| | | Single nucleotide variant (nonsense) | Hereditary cancer-predisposing syndrome +1 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (nonsense) | Hereditary cancer-predisposing syndrome +1 more | GPathogenic/Likely pathogenic |
| | RAD51D, RAD51L3-RFFL (Q60*) | Single nucleotide variant (nonsense +1 more) | Hereditary cancer-predisposing syndrome +1 more | |
| | | Single nucleotide variant (nonsense) | Hereditary cancer-predisposing syndrome | |
| | | Single nucleotide variant (nonsense) | not provided +2 more | GPathogenic/Likely pathogenic |
| | | Deletion (nonsense +1 more) | Hereditary nonpolyposis colorectal neoplasms +1 more | |
| | | Single nucleotide variant (splice acceptor variant) | Familial cancer of breast +1 more | |
| | | Single nucleotide variant (splice donor variant +1 more) | Familial cancer of breast +1 more | |
| | | Single nucleotide variant (nonsense +1 more) | Breast-ovarian cancer, familial, susceptibility to, 1 | |
| | | Deletion (frameshift variant) | Lynch syndrome +3 more | GPathogenic/Likely pathogenic |
| | | Microsatellite (frameshift variant) | Familial cancer of breast +3 more | |
| | | Deletion (frameshift variant) | Fanconi anemia complementation group J +3 more | |
| | | Duplication (frameshift variant +1 more) | Lynch syndrome 5 +4 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (splice donor variant +1 more) | Breast-ovarian cancer, familial, susceptibility to, 1 +1 more | |
| | | Deletion (frameshift variant) | Breast-ovarian cancer, familial, susceptibility to, 2 | |
| | | Single nucleotide variant (nonsense +1 more) | Breast-ovarian cancer, familial, susceptibility to, 1 | |
| | | Single nucleotide variant (nonsense) | not provided +3 more | |
| | | Deletion (frameshift variant) | Breast-ovarian cancer, familial, susceptibility to, 2 | |
| | | Deletion (intron variant) | Ataxia-telangiectasia syndrome +3 more | GPathogenic/Likely pathogenic |
| | | Deletion (nonsense) | Fanconi anemia complementation group J +4 more | GPathogenic/Likely pathogenic |
| | | Deletion (frameshift variant +1 more) | Hereditary cancer-predisposing syndrome +3 more | GConflicting classifications of pathogenicity |
| | | Deletion (frameshift variant) | Hereditary cancer-predisposing syndrome +4 more | |
| | | Deletion (5 prime UTR variant +1 more) | Hereditary cancer-predisposing syndrome +3 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (nonsense) | Familial cancer of breast +1 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (splice donor variant +1 more) | Breast-ovarian cancer, familial, susceptibility to, 4 +2 more | GConflicting classifications of pathogenicity |
| | | Microsatellite (frameshift variant +1 more) | not provided +2 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (nonsense) | Hereditary cancer-predisposing syndrome +2 more | |
| | | Single nucleotide variant (missense variant +1 more) | Hereditary cancer-predisposing syndrome +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | Ataxia-telangiectasia syndrome +3 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (nonsense) | MSH6-related disorder +4 more | GPathogenic/Likely pathogenic |
| | | Deletion (splice donor variant) | Hereditary breast ovarian cancer syndrome +4 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | not provided +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Lynch syndrome 1 | |
| | | Single nucleotide variant (splice donor variant) | Hereditary cancer-predisposing syndrome +4 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant +1 more) | PTEN hamartoma tumor syndrome | |
| | | Single nucleotide variant (nonsense +2 more) | Familial cancer of breast +3 more | |
| | | Single nucleotide variant (intron variant +2 more) | not provided +2 more | |
| | | Single nucleotide variant (missense variant +1 more) | Ataxia-telangiectasia syndrome +5 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (synonymous variant) | Li-Fraumeni syndrome 1 +7 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (nonsense) | Breast-ovarian cancer, familial, susceptibility to, 2 | |
| | | Single nucleotide variant (missense variant) | Li-Fraumeni syndrome 1 | |
| | | Single nucleotide variant (missense variant +1 more) | Hereditary cancer-predisposing syndrome +5 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (nonsense) | Fanconi anemia complementation group J +4 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Li-Fraumeni syndrome +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | PTEN hamartoma tumor syndrome | |
| | | Duplication (frameshift variant) | not provided +4 more | GPathogenic/Likely pathogenic |
| | | Deletion (splice acceptor variant) | Breast-ovarian cancer, familial, susceptibility to, 3 +5 more | GPathogenic/Likely pathogenic |
| | RAD51D, RAD51L3-RFFL (Q151* +1 more) | Single nucleotide variant (nonsense +2 more) | Hereditary cancer-predisposing syndrome +3 more | GPathogenic/Likely pathogenic |
| | | Deletion (frameshift variant) | Familial cancer of breast +1 more | |
| | | Single nucleotide variant (splice donor variant) | Ataxia-telangiectasia syndrome +4 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (nonsense) | Hereditary cancer-predisposing syndrome +3 more | |
| | | Duplication (frameshift variant) | Nijmegen breakage syndrome-like disorder +2 more | |
| | | Deletion (intron variant) | Hereditary cancer-predisposing syndrome +5 more | GPathogenic/Likely pathogenic |
| | | Duplication (frameshift variant) | Familial cancer of breast +4 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Hereditary cancer-predisposing syndrome +6 more | |
| | | Single nucleotide variant (missense variant) | not specified +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (splice donor variant) | Li-Fraumeni syndrome 2 +11 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant +1 more) | Li-Fraumeni syndrome 2 +10 more | GConflicting classifications of pathogenicity |