| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | | Copy number gain | See cases | |
| | CD27, CD27-AS1 +1 more (Q181*) | Single nucleotide variant (non-coding transcript variant +1 more) | not provided +1 more | GConflicting classifications of pathogenicity |
| | CD27, CD27-AS1 +1 more (I190fs) | Indel (frameshift variant +1 more) | not provided | |
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