| | LOC130062145, NDUFV2 (F3S) | Single nucleotide variant (missense variant) | not provided +1 more | |
| | LOC130062145, NDUFV2 (S4F) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (intron variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | NDUFV2, NDUFV2-AS1 (V107I) | Single nucleotide variant (missense variant) | Inborn genetic diseases +1 more | |
| | NDUFV2, NDUFV2-AS1 (P108T) | Single nucleotide variant (missense variant) | not provided +1 more | |
| | NDUFV2, NDUFV2-AS1 (G157E) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | NDUFV2, NDUFV2-AS1 (P165fs) | Insertion (frameshift variant) | Inborn genetic diseases | |
| | NDUFV2, NDUFV2-AS1 (D166G) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | NDUFV2, NDUFV2-AS1 (L168P) | Single nucleotide variant (missense variant) | not provided +1 more | |
| | NDUFV2, NDUFV2-AS1 (N191S) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | NDUFV2, NDUFV2-AS1 (Y193N) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | NDUFV2, NDUFV2-AS1 (I205T) | Single nucleotide variant (missense variant) | not provided +1 more | |
| | NDUFV2-AS1, NDUFV2 (A210P) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | NDUFV2, NDUFV2-AS1 (S220N) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | NDUFV2, NDUFV2-AS1 (P227L) | Single nucleotide variant (missense variant) | not provided +1 more | |