| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | | Single nucleotide variant (missense variant +2 more) | GRAP-related disorder | |
| | | Single nucleotide variant (missense variant +2 more) | GRAP-related disorder | |
| | | Single nucleotide variant (synonymous variant +1 more) | GRAP-related disorder | |
| | GRAP, SLC5A10 (R197Q +1 more) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | GRAP, SLC5A10 (A160V +1 more) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | GRAP, SLC5A10 (A122P +1 more) | Single nucleotide variant (missense variant +1 more) | not specified | |
Click to view in NCBI Gene