| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | HAGHL, LOC130058133 (C144F) | Single nucleotide variant (missense variant) | not specified | |
| | HAGHL, LOC130058132 (L85P) | Single nucleotide variant (missense variant) | not specified | |
| | HAGHL, LOC130058132 (L76P) | Single nucleotide variant (missense variant) | not specified | |
| | HAGHL, LOC130058133 (S143W) | Single nucleotide variant (missense variant) | not specified | |
| | HAGHL, LOC130058132 (H101Q) | Single nucleotide variant (missense variant) | not specified | |
| | HAGHL, LOC130058131 (D58N) | Single nucleotide variant (missense variant) | not specified | |
| | HAGHL, LOC130058131 (P64A) | Single nucleotide variant (missense variant) | not specified | |
| | HAGHL, LOC130058132 (D79G) | Single nucleotide variant (missense variant) | not specified | |
| | HAGHL, LOC130058132 (I100V) | Single nucleotide variant (missense variant) | not specified | |
| | HAGHL, LOC130058132 (D79A) | Single nucleotide variant (missense variant) | not specified | |
| | HAGHL, LOC130058133 (S137W) | Single nucleotide variant (missense variant) | not specified | |
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