| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | CUBN, LOC126860871 (R235*) | Single nucleotide variant (nonsense) | Proteinuria, chronic benign +2 more | GPathogenic/Likely pathogenic |
| | CUBN, LOC126860871 (R224H) | Single nucleotide variant (missense variant) | Imerslund-Grasbeck syndrome type 1 +2 more | |
| | CUBN, LOC126860871 (T205M) | Single nucleotide variant (missense variant) | Inborn genetic diseases +3 more | |
Click to view in NCBI Gene