| | LOC112533659, LOC112533660 +2032 more | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number loss | See cases | |
| | COX11, LOC129390891 +5 more | Copy number gain | See cases | |
| | COX11, TOM1L1 (I386T +1 more) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Single nucleotide variant (missense variant +2 more) | not specified | |
| | | Single nucleotide variant (missense variant +2 more) | Mitochondrial complex IV deficiency, nuclear type 23 | |
| | | Duplication (frameshift variant +2 more) | Mitochondrial complex IV deficiency, nuclear type 23 | |
| | | Single nucleotide variant (missense variant +2 more) | not specified | |
| | | Single nucleotide variant (missense variant +2 more) | Mitochondrial complex IV deficiency, nuclear type 23 | |
| | | Single nucleotide variant (missense variant +2 more) | Mitochondrial complex IV deficiency, nuclear type 23 | |
| | | Single nucleotide variant (missense variant +2 more) | Mitochondrial complex IV deficiency, nuclear type 23 | |
| | | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Indel (frameshift variant +1 more) | Mitochondrial complex IV deficiency, nuclear type 23 | |
| | | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Copy number gain | not provided | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |