| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | DAPK1, LOC126860671 (C959S) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | DAPK1, LOC126860671 (N980S) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | DAPK1, LOC126860671 (Q989H) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | DAPK1, LOC126860671 (E1020K) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
Click to view in NCBI Gene