| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | RAD51D, RAD51L3-RFFL (D310A +2 more) | Single nucleotide variant (missense variant +1 more) | Hereditary cancer-predisposing syndrome +1 more | |
| | RAD51D, RAD51L3-RFFL (T280S +2 more) | Single nucleotide variant (non-coding transcript variant +1 more) | Hereditary cancer-predisposing syndrome +2 more | GConflicting classifications of pathogenicity |
| | RAD51D, RAD51L3-RFFL (S207L +2 more) | Single nucleotide variant (non-coding transcript variant +1 more) | not provided +4 more | GConflicting classifications of pathogenicity |
| | RAD51D, RAD51L3-RFFL (R186* +2 more) | Single nucleotide variant (nonsense +1 more) | Hereditary cancer-predisposing syndrome +3 more | |
| | RAD51D, RAD51L3-RFFL (Q160* +1 more) | Single nucleotide variant (nonsense +2 more) | not provided +2 more | |
| | RAD51D, RAD51L3-RFFL (A122fs +1 more) | Deletion (frameshift variant +2 more) | not provided +3 more | GPathogenic/Likely pathogenic |
| | RAD51D, RAD51L3-RFFL (G130fs +1 more) | Duplication (frameshift variant +2 more) | not provided +2 more | |
| | RAD51L3-RFFL, RAD51D (R55W) | Single nucleotide variant (missense variant +1 more) | not provided +3 more | GConflicting classifications of pathogenicity |
| | RAD51D, RAD51L3-RFFL (M1L) | Single nucleotide variant (missense variant +2 more) | not specified +3 more | GConflicting classifications of pathogenicity |
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