| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | ATP5MG, LOC100131626 (L27S) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | ATP5MG, LOC100131626 (L27M) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | ATP5MG, LOC100131626 (R26L) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | ATP5MG, LOC100131626 (P13L) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | ATP5MG, LOC100131626 (E10A) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | ATP5MG, LOC100131626 (R96W) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | ATP5MG, LOC100131626 (T62S) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | ATP5MG, LOC100131626 (I50T) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | ATP5MG, LOC100131626 (P43H) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | ATP5MG, LOC100131626 (N58S) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | ATP5MG, LOC100131626 (V79M) | Single nucleotide variant (missense variant +1 more) | not specified | |
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