| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC122817718, MAP4K4 (A660S +41 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | LOC122817718, MAP4K4 (E657D +41 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | LOC122817718, MAP4K4 (T515M +41 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | MAP4K4, LOC122817718 (T495M +41 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | MAP4K4, LOC122817718 (A737T +41 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
Click to view in NCBI Gene