| | LOC119369030, PPP1R15A (P3S) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | PPP1R15A, LOC119369030 (L28F) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC119369030, PPP1R15A (P41S) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC119369030, PPP1R15A (V56I) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC119369030, PPP1R15A (A64V) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC119369030, PPP1R15A (R65M) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC119369030, PPP1R15A (T73I) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC119369030, LOC119369031 +1 more (G129R) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC119369030, LOC119369031 +1 more (R139C) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC119369030, LOC119369031 +1 more (P144A) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC119369030, LOC119369031 +1 more (V168F) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC119369030, LOC119369031 +1 more (E170V) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC119369030, PPP1R15A (V190M) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC119369030, LOC119369031 +1 more (P217L) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC119369030, LOC119369031 +1 more (S222C) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC119369030, LOC119369031 +1 more (V248M) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC119369030, PPP1R15A (R263C) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC119369030, PPP1R15A (A294V) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC119369030, PPP1R15A (L299P) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC119369030, PPP1R15A (G318R) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC119369030, PPP1R15A (C328R) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC119369030, PPP1R15A (F338L) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC119369030, LOC119369032 +1 more (S388F) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |