| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC130005396, SERGEF (W20S) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | LOC130005396, SERGEF (A19V) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | LOC130005396, SERGEF (F18C) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | LOC130005396, SERGEF (A11T) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | LOC130005396, SERGEF (E4K) | Single nucleotide variant (missense variant +1 more) | not specified | |
Click to view in NCBI Gene