| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | LOC126861153, SPTY2D1 (T198S) | Single nucleotide variant (missense variant) | not specified | |
| | LOC126861153, SPTY2D1 (F181L) | Single nucleotide variant (missense variant) | not specified | |
| | LOC126861153, SPTY2D1 (S113T) | Single nucleotide variant (missense variant) | not specified | |
| | LOC126861153, SPTY2D1 (R205Q) | Single nucleotide variant (missense variant) | not specified | |
| | LOC126861153, SPTY2D1 (V152A) | Single nucleotide variant (missense variant) | not specified | |
| | LOC126861153, SPTY2D1 (I101V) | Single nucleotide variant (missense variant) | not provided | |
| | LOC126861153, SPTY2D1 (Y143C) | Single nucleotide variant (missense variant) | not specified | |
| | LOC126861153, SPTY2D1 (R174S) | Single nucleotide variant (missense variant) | not specified | |
| | LOC126861153, SPTY2D1 (R65K) | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | not specified | |
| | LOC126861153, SPTY2D1 (M125T) | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | not specified | |
| | LOC126861153, SPTY2D1 (A199T) | Single nucleotide variant (missense variant) | not specified | |
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