| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (synonymous variant +1 more) | not provided +3 more | |
| | | Microsatellite (frameshift variant) | Methylcobalamin deficiency type cblG +1 more | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases +3 more | |
| | | Deletion (frameshift variant) | Methylcobalamin deficiency type cblG +1 more | |
Click to view in NCBI Gene