| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | C16orf92, TLCD3B (Q269R +2 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | C16orf92, TLCD3B (P115L +2 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | C16orf92, TLCD3B (A197V +2 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | C16orf92, TLCD3B (D59N +2 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
Click to view in NCBI Gene