| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | CAPN10, LOC112840920 (F14L) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | CAPN10, LOC112840920 (A3V) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | CAPN10, LOC112840920 (P46S) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | CAPN10, LOC112840920 (P9S) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | CAPN10, LOC112840920 (T42M) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | CAPN10, LOC112840920 (L34V) | Single nucleotide variant (missense variant) | not provided | |
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