| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | | Single nucleotide variant (missense variant +1 more) | not specified +3 more | |
| | | Single nucleotide variant (missense variant +1 more) | not specified +3 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | not specified +3 more | |
| | | Duplication (intron variant) | not provided +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | Methylcobalamin deficiency type cblE +3 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Disorders of Intracellular Cobalamin Metabolism +3 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | not specified +3 more | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | Methylcobalamin deficiency type cblE +3 more | |
Click to view in NCBI Gene