| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | CENPV, LOC130060319 (P61L) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | CENPV, LOC130060319 (E54K) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | CENPV, LOC130060319 (T37I) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | CENPV, LOC130060319 (A31V) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | CENPV, LOC130060319 (A28P) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | CENPV, LOC130060319 (A25E) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | CENPV, LOC130060319 (G19A) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
Click to view in NCBI Gene