| | | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Single nucleotide variant (3 prime UTR variant +2 more) | not specified | |
| | | Single nucleotide variant (3 prime UTR variant +2 more) | not specified | |
| | LOC113788297, NDUFAF6 (W10S) | Single nucleotide variant (5 prime UTR variant +3 more) | Inborn genetic diseases | |
| | LOC113788297, NDUFAF6 (L65P) | Single nucleotide variant (5 prime UTR variant +3 more) | Inborn genetic diseases | |
| | LOC113788297, NDUFAF6 (A3V) | Single nucleotide variant (5 prime UTR variant +3 more) | Inborn genetic diseases | |
| | LOC113788297, NDUFAF6 (P25S) | Single nucleotide variant (5 prime UTR variant +3 more) | not provided | |
| | LOC113788297, NDUFAF6 (C61Y) | Single nucleotide variant (5 prime UTR variant +3 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (3 prime UTR variant +2 more) | not specified | |
| | | Single nucleotide variant (3 prime UTR variant +2 more) | not specified | |
| | | Single nucleotide variant (3 prime UTR variant +2 more) | not specified | |
| | | Single nucleotide variant (3 prime UTR variant +2 more) | not specified | |
| | | Single nucleotide variant (3 prime UTR variant +2 more) | not specified | |
| | | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Single nucleotide variant (5 prime UTR variant +3 more) | NDUFAF6-related disorder | |
| | | Single nucleotide variant (5 prime UTR variant +3 more) | not provided | |
| | LOC113788297, NDUFAF6 (E63*) | Single nucleotide variant (5 prime UTR variant +3 more) | not provided | |
| | LOC113788297, NDUFAF6 (S50R) | Single nucleotide variant (5 prime UTR variant +3 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Single nucleotide variant (missense variant +1 more) | not specified | |
| | LOC113788297, NDUFAF6 (P37L) | Single nucleotide variant (5 prime UTR variant +3 more) | not provided | |
| | LOC113788297, NDUFAF6 (M1L) | Single nucleotide variant (5 prime UTR variant +4 more) | not provided | |
| | LOC113788297, NDUFAF6 (P12Q) | Single nucleotide variant (5 prime UTR variant +3 more) | Inborn genetic diseases | |
| | LOC113788297, NDUFAF6 (G19D) | Single nucleotide variant (5 prime UTR variant +3 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Single nucleotide variant (3 prime UTR variant +2 more) | not specified | |
| | | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Single nucleotide variant (missense variant +1 more) | not specified | |
| | LOC113788297, NDUFAF6 (C22Y) | Single nucleotide variant (5 prime UTR variant +3 more) | Inborn genetic diseases | |
| | LOC113788297, NDUFAF6 (P18L) | Single nucleotide variant (5 prime UTR variant +3 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (3 prime UTR variant +2 more) | not specified | |
| | LOC113788297, NDUFAF6 (D58N) | Single nucleotide variant (5 prime UTR variant +3 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Single nucleotide variant (3 prime UTR variant +2 more) | not specified | |
| | | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Single nucleotide variant (missense variant +1 more) | not specified | |
| | LOC113788297, NDUFAF6 (P18S) | Single nucleotide variant (5 prime UTR variant +3 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (3 prime UTR variant +2 more) | not specified | |
| | | Single nucleotide variant (3 prime UTR variant +2 more) | not specified | |
| | LOC113788297, NDUFAF6 (L15F) | Single nucleotide variant (5 prime UTR variant +3 more) | not provided | |
| | | Single nucleotide variant (5 prime UTR variant +3 more) | not provided | |
| | LOC113788297, NDUFAF6 (H6Q) | Single nucleotide variant (5 prime UTR variant +3 more) | not provided | |
| | LOC113788297, NDUFAF6 (R14L) | Single nucleotide variant (5 prime UTR variant +3 more) | not provided | |
| | LOC113788297, NDUFAF6 (R23C) | Single nucleotide variant (non-coding transcript variant +3 more) | not provided | |
| | | Single nucleotide variant (5 prime UTR variant +3 more) | not provided | |
| | LOC113788297, NDUFAF6 (A31P) | Single nucleotide variant (5 prime UTR variant +3 more) | not provided | |
| | | Single nucleotide variant (5 prime UTR variant +3 more) | not provided | |
| | | Single nucleotide variant (5 prime UTR variant +3 more) | not provided | |
| | LOC113788297, NDUFAF6 (G28R) | Single nucleotide variant (5 prime UTR variant +3 more) | not provided +1 more | |
| | LOC113788297, NDUFAF6 (G51R) | Single nucleotide variant (5 prime UTR variant +3 more) | not provided | |
| | LOC113788297, NDUFAF6 (S50fs) | Deletion (5 prime UTR variant +3 more) | not provided | |
| | | Single nucleotide variant (5 prime UTR variant +3 more) | not provided | |
| | LOC113788297, NDUFAF6 (G51*) | Single nucleotide variant (5 prime UTR variant +3 more) | not provided | |
| | | Single nucleotide variant (5 prime UTR variant +3 more) | not provided | |
| | LOC113788297, NDUFAF6 (G7A) | Single nucleotide variant (5 prime UTR variant +3 more) | not provided +1 more | |
| | LOC113788297, NDUFAF6 (R14P) | Single nucleotide variant (5 prime UTR variant +3 more) | not provided | |
| | LOC113788297, NDUFAF6 (S4Y) | Single nucleotide variant (5 prime UTR variant +3 more) | not provided | |
| | LOC113788297, NDUFAF6 (S8P) | Single nucleotide variant (5 prime UTR variant +3 more) | not provided | |
| | | Single nucleotide variant | not provided | |
| | LOC113788297, NDUFAF6 (R35Q) | Single nucleotide variant (5 prime UTR variant +3 more) | not provided | |
| | LOC113788297, NDUFAF6 (W10*) | Single nucleotide variant (5 prime UTR variant +3 more) | not provided | |
| | LOC113788297, NDUFAF6 (G11E) | Single nucleotide variant (5 prime UTR variant +3 more) | not provided | |
| | | Single nucleotide variant (5 prime UTR variant +3 more) | not provided | |
| | LOC113788297, NDUFAF6 (G38R) | Single nucleotide variant (5 prime UTR variant +3 more) | Inborn genetic diseases +1 more | |
| | LOC113788297, NDUFAF6 (G7V) | Single nucleotide variant (5 prime UTR variant +3 more) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (5 prime UTR variant +3 more) | not provided | |
| | LOC113788297, NDUFAF6 (G43E) | Single nucleotide variant (5 prime UTR variant +3 more) | not provided | |
| | LOC113788297, NDUFAF6 (R32H) | Single nucleotide variant (5 prime UTR variant +3 more) | not provided | |
| | LOC113788297, NDUFAF6 (A31G) | Single nucleotide variant (5 prime UTR variant +3 more) | not provided +1 more | |
| | LOC113788297, NDUFAF6 (A3G) | Single nucleotide variant (5 prime UTR variant +3 more) | Leigh syndrome | |
| | | Single nucleotide variant (5 prime UTR variant +3 more) | not provided | |
| | | Single nucleotide variant (5 prime UTR variant +3 more) | not provided | |
| | LOC113788297, NDUFAF6 (M33V) | Single nucleotide variant (5 prime UTR variant +3 more) | not provided | |
| | LOC113788297, NDUFAF6 (P39L) | Single nucleotide variant (5 prime UTR variant +3 more) | Leigh syndrome | |
| | | Single nucleotide variant (missense variant +1 more) | Leigh syndrome | |
| | | Single nucleotide variant (5 prime UTR variant +2 more) | not provided | |
| | | Single nucleotide variant (intron variant) | not specified | |
| | | Single nucleotide variant (5 prime UTR variant +3 more) | not specified | |
| | LOC113788297, NDUFAF6 (S42fs) | Microsatellite (5 prime UTR variant +3 more) | not provided | |
| | | Single nucleotide variant (nonsense +2 more) | Not Specified | Gno classification for the single variant Sno classification for the single variant Ono classification for the single variant |
| | | Single nucleotide variant (missense variant +1 more) | Not Specified | Gno classification for the single variant Sno classification for the single variant Ono classification for the single variant |
| | LOC113788297, NDUFAF6 (M1T) | Single nucleotide variant (5 prime UTR variant +4 more) | Inborn genetic diseases +1 more | |
| | | Single nucleotide variant (non-coding transcript variant +3 more) | not specified | |
| | | Single nucleotide variant (intron variant) | not specified | |
| | | Single nucleotide variant (intron variant) | not specified | |
| | LOC113788297, NDUFAF6 (A47T) | Single nucleotide variant (non-coding transcript variant +3 more) | not specified | |
| | LOC113788297, NDUFAF6 (G28A) | Single nucleotide variant (5 prime UTR variant +3 more) | NDUFAF6-related disorder +4 more | |
| | | Single nucleotide variant (5 prime UTR variant +3 more) | not provided +1 more | |
| | | Single nucleotide variant (intron variant) | not specified | |