| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | GCNA, LOC125467762 (R632H) | Single nucleotide variant (missense variant) | not specified | |
| | GCNA, LOC125467762 (D611E) | Single nucleotide variant (missense variant) | not specified | |
| | GCNA, LOC125467762 (T651M) | Single nucleotide variant (missense variant) | not specified | |
| | | Indel | Spermatogenic failure, X-linked, 4 | |
Click to view in NCBI Gene