| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC126862575, MAP3K14
+1 more (N812K) | Single nucleotide variant (missense variant) | not specified | |
| | LOC126862575, MAP3K14
+1 more (T764I) | Single nucleotide variant (missense variant) | not specified | |
| | LOC126862575, MAP3K14
+1 more (P750A) | Single nucleotide variant (missense variant) | not specified | |
| | LOC126862575, MAP3K14
+1 more (P716T) | Single nucleotide variant (missense variant) | not specified | |
| | LOC126862575, MAP3K14
+1 more (P716A) | Single nucleotide variant (missense variant) | not specified | |
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