| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | RANBP2, SEPTIN10 (Q112H +9 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | RANBP2, SEPTIN10 (V260I +9 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | RANBP2, SEPTIN10 (K106N +9 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | RANBP2, SEPTIN10 (M223V +9 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | RANBP2, SEPTIN10 (F259L +9 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | RANBP2, SEPTIN10 (I17M +9 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | RANBP2, SEPTIN10 (N154D +7 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | RANBP2, SEPTIN10 (G168D +6 more) | Single nucleotide variant (missense variant +2 more) | Inborn genetic diseases | |
| | RANBP2, SEPTIN10 (F146L +6 more) | Single nucleotide variant (missense variant +2 more) | Inborn genetic diseases | |
| | RANBP2, SEPTIN10 (L50V +5 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | RANBP2, SEPTIN10 (Q31R +5 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | RANBP2, SEPTIN10 (S8L +4 more) | Single nucleotide variant (missense variant +2 more) | Inborn genetic diseases | |
| | RANBP2, SEPTIN10 (T9M +2 more) | Single nucleotide variant (5 prime UTR variant +2 more) | Inborn genetic diseases | |
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