| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | CCNC, TSTD3 (V91G +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | not specified | |
| | CCNC, TSTD3 (K171Q +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | CCNC, TSTD3 (Q209H +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | CCNC, TSTD3 (Y37F +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | CCNC, TSTD3 (V30I +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | not specified | |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | not specified | |
| | CCNC, TSTD3 (T167A +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | | Duplication (intron variant) | CIC-rearranged sarcoma | |
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