| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | CAP2, LOC101928491 (A162T +1 more) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | CAP2, LOC101928491 (R125W +1 more) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | CAP2, LOC101928491 (V148A +1 more) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | CAP2, LOC101928491 (I117N +1 more) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | CAP2, LOC101928491 (S108L +1 more) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | CAP2, LOC101928491 (V122L +1 more) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | CAP2, LOC101928491 (V170I +1 more) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | LOC101928491, CAP2 (V110I +1 more) | Single nucleotide variant (missense variant +1 more) | not provided | |
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