| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | | Single nucleotide variant (intron variant) | Breast-ovarian cancer, familial, susceptibility to, 4 +3 more | GConflicting classifications of pathogenicity |
| | RAD51D, RAD51L3-RFFL (R266C +2 more) | Single nucleotide variant (non-coding transcript variant +1 more) | Breast-ovarian cancer, familial, susceptibility to, 4 +6 more | GConflicting classifications of pathogenicity |
| | RAD51L3-RFFL, RAD51D (R232* +2 more) | Single nucleotide variant (nonsense +1 more) | Colorectal cancer +5 more | GPathogenic/Likely pathogenic |
| | RAD51D, RAD51L3-RFFL (S207L +2 more) | Single nucleotide variant (non-coding transcript variant +1 more) | not provided +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | Breast-ovarian cancer, familial, susceptibility to, 4 +1 more | GConflicting classifications of pathogenicity |
| | RAD51L3-RFFL, RAD51D (R165Q +2 more) | Single nucleotide variant (non-coding transcript variant +1 more) | not specified +3 more | |
| | RAD51D, RAD51L3-RFFL (Q151* +1 more) | Single nucleotide variant (nonsense +2 more) | Hereditary cancer-predisposing syndrome +3 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (splice acceptor variant +1 more) | Hereditary cancer-predisposing syndrome +1 more | GPathogenic/Likely pathogenic |
| | RAD51D, RAD51L3-RFFL (A80V) | Single nucleotide variant (missense variant +1 more) | Hereditary cancer-predisposing syndrome +1 more | |
Click to view in NCBI Gene