| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | LOC130065317, MRPS26 (R3G) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC130065317, MRPS26 (T12P) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC130065317, MRPS26 (P16S) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC130065317, MRPS26 (R17Q) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC130065317, MRPS26 (E40K) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC130065317, MRPS26 (V42M) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC130065317, MRPS26 (V42L) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | MRPS26, LOC130065317 (H117Q) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | 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