| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC126862575, MAP3K14
+1 more (N812K) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC126862575, MAP3K14
+1 more (P750A) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC126862575, MAP3K14
+1 more (P716A) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
Click to view in NCBI Gene