| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (synonymous variant +1 more) | TARS1-related condition | |
| | LOC126807348, TARS1 (T441I +2 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | LOC126807348, TARS1 (M419V +2 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Copy number loss | not provided | |
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