| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | EEF2, LOC130063169 (V747M) | Single nucleotide variant (missense variant) | not specified | |
| | EEF2, LOC130063169 (H705Y) | Single nucleotide variant (missense variant) | not specified +1 more | |
| | EEF2, LOC130063169 (G699S) | Single nucleotide variant (missense variant) | not specified | |
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