| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | JCAD, LOC130003583 (P791S +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | JCAD, LOC130003584 (E845G +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 | |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | not provided | |
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