| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | CPNE6, LOC126861900 (R332Q +1 more) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | CPNE6, LOC126861900 (R387G +1 more) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | CPNE6, LOC126861900 (E441Q +1 more) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | CPNE6, LOC126861900 (R411Q +1 more) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | CPNE6, LOC126861900 (D381E +1 more) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | CPNE6, LOC126861900 (R535Q +1 more) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | CPNE6, LOC126861900 (R425G +1 more) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | CPNE6, LOC126861900 (G485S +1 more) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | CPNE6, LOC126861900 (E426K +1 more) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | CPNE6, LOC126861900 (R387P +1 more) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | CPNE6, LOC126861900 (N317S +1 more) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | CPNE6, LOC126861900 (F507V +1 more) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | CPNE6, LOC126861900 (T294I +1 more) | Single nucleotide variant (missense variant +1 more) | not provided | |
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