| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | HOXC4, HOXC5 +1 more (G25R) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | HOXC4, HOXC5 +1 more (A92V) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | HOXC4, HOXC5 +1 more (Y99N) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | HOXC4, HOXC5 +1 more (P135T) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
Click to view in NCBI Gene