| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | NDUFC2-KCTD14, THRSP (A111T) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | NDUFC2-KCTD14, THRSP (R19Q) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | NDUFC2-KCTD14, THRSP (W80R) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | NDUFC2-KCTD14, THRSP (E94D) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | NDUFC2-KCTD14, THRSP (V40M) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | NDUFC2-KCTD14, THRSP (K10R) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | NDUFC2-KCTD14, THRSP (R77W) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | NDUFC2-KCTD14, THRSP (R38W) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | NDUFC2-KCTD14, THRSP (V31A) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | NDUFC2-KCTD14, THRSP (T142M) | Single nucleotide variant (missense variant +1 more) | not provided | |
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