| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | RAD51D, RAD51L3-RFFL (R291H +2 more) | Single nucleotide variant (non-coding transcript variant +1 more) | not specified +3 more | |
| | RAD51D, RAD51L3-RFFL (R291C +2 more) | Single nucleotide variant (non-coding transcript variant +1 more) | not specified +3 more | |
| | RAD51D, RAD51L3-RFFL (R266C +2 more) | Single nucleotide variant (non-coding transcript variant +1 more) | not provided +6 more | GConflicting classifications of pathogenicity |
| | RAD51D, RAD51L3-RFFL (R253* +2 more) | Single nucleotide variant (non-coding transcript variant +1 more) | not provided +2 more | GConflicting classifications of pathogenicity |
| | RAD51D, RAD51L3-RFFL (R232* +2 more) | Single nucleotide variant (nonsense +1 more) | Diffuse midline glioma, H3 K27-altered +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) | not provided | |
| | RAD51D, RAD51L3-RFFL (D90G) | Single nucleotide variant (missense variant +1 more) | not specified +4 more | |
| | RAD51D, RAD51L3-RFFL (C9S) | Single nucleotide variant (missense variant +1 more) | Hereditary cancer-predisposing syndrome +6 more | GConflicting classifications of pathogenicity |
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