| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (missense variant) | Methylmalonic aciduria and homocystinuria type cblF | |
| | | Deletion (frameshift variant) | Inborn genetic diseases +3 more | |
| | | Single nucleotide variant (intron variant) | not specified +1 more | |
| | | Single nucleotide variant (synonymous variant) | Methylmalonic aciduria and homocystinuria type cblF +1 more | |
| | | Single nucleotide variant (intron variant) | Methylmalonic aciduria and homocystinuria type cblF | |
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