| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | LOC126861077, TEX36 (R59Q) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC126861077, TEX36 (P39L) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC126861077, TEX36 (S36P) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
Click to view in NCBI Gene