| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | LOC130065998, TP53RK +1 more | Single nucleotide variant (synonymous variant +1 more) | TP53RK-related disorder | |
| | LOC130065998, TP53RK +1 more | Single nucleotide variant (synonymous variant +1 more) | not provided +1 more | |
| | LOC130065998, TP53RK +1 more (T8M) | Single nucleotide variant (missense variant) | not provided +1 more | |
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