| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | CACFD1, LOC130002915 (G170R +3 more) | Single nucleotide variant (missense variant) | not specified | |
| | CACFD1, LOC130002915 (A177V +1 more) | Single nucleotide variant (3 prime UTR variant +1 more) | not specified | |
| | CACFD1, LOC130002915 (C230Y +1 more) | Single nucleotide variant (3 prime UTR variant +1 more) | not specified | |
| | CACFD1, LOC130002915 (R169T +3 more) | Single nucleotide variant (missense variant) | not specified | |
| | CACFD1, LOC130002915 (S164L +1 more) | Single nucleotide variant (synonymous variant +1 more) | not specified | |
Click to view in NCBI Gene