| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (synonymous variant +1 more) | not provided | |
| | | Single nucleotide variant (3 prime UTR variant +2 more) | not provided | |
| | | Copy number loss | not provided | |
| | TMEM88B, TNFRSF14
+79 more | Copy number loss | not provided | |
Click to view in NCBI Gene