| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Insertion (frameshift variant +1 more) | Hereditary cancer-predisposing syndrome +2 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (nonsense) | Fanconi anemia complementation group O +3 more | |
| | LOC129390903, RAD51C (Q222*) | Single nucleotide variant (nonsense +1 more) | Breast and/or ovarian cancer | |
| | | Deletion (splice acceptor variant) | Hereditary cancer-predisposing syndrome +5 more | GPathogenic/Likely pathogenic |
| | | Deletion (intron variant) | not provided +5 more | GPathogenic/Likely pathogenic |
Click to view in NCBI Gene