| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC129998941, PPP1R35 (D51N) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC129998941, PPP1R35 (A127G) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC129998941, PPP1R35 (K64R) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC129998941, PPP1R35 (E132D) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC129998941, PPP1R35 (S137L) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC129998941, PPP1R35 (R141P) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | PPP1R35, PPP1R35-AS1 (E16K) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC129998941, PPP1R35 (P98L) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC129998941, PPP1R35 (E115K) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Deletion (frameshift variant +1 more) | See cases | |
Click to view in NCBI Gene