| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | RAD51D, RAD51L3-RFFL (I311N +2 more) | Single nucleotide variant (missense variant +1 more) | not specified +6 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | not provided | |
| | RAD51D, RAD51L3-RFFL (E233G +2 more) | Single nucleotide variant (non-coding transcript variant +1 more) | not specified +3 more | |
| | RAD51D, RAD51L3-RFFL (R232Q +2 more) | Single nucleotide variant (non-coding transcript variant +1 more) | Breast and/or ovarian cancer +4 more | |
| | RAD51L3-RFFL, RAD51D (R165Q +2 more) | Single nucleotide variant (non-coding transcript variant +1 more) | not specified +3 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Hereditary cancer-predisposing syndrome +3 more | |
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