| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | LRTOMT, TOMT (R29C +1 more) | Single nucleotide variant (missense variant +1 more) | not provided +1 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Autosomal recessive nonsyndromic hearing loss 63 +2 more | GConflicting classifications of pathogenicity |
| | TOMT, ANAPC15 +1 more (A133P +2 more) | Single nucleotide variant (missense variant +3 more) | Autosomal recessive nonsyndromic hearing loss 63 +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant +3 more) | LRTOMT-related disorder | |
| | ANAPC15, LRTOMT +1 more (T168M +2 more) | Single nucleotide variant (missense variant +3 more) | LRTOMT-related disorder +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant +3 more) | LRTOMT-related disorder +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided +1 more | |
Click to view in NCBI Gene