PPM1H
protein phosphatase, Mg2+/Mn2+ dependent 1H
Summary
Enables identical protein binding activity and phosphoprotein phosphatase activity. Predicted to be involved in signal transduction. Located in cytoplasm and nucleoplasm. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants35 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs752870905 | 12:63,042,352 | G/A | — | uncertain significance |
| rs540042623 | 12:63,042,384 | C/T | — | uncertain significance |
| rs776028923 | 12:63,042,405 | G/A | — | uncertain significance |
| rs747764925 | 12:63,042,406 | C/A | — | uncertain significance |
| rs371293545 | 12:63,042,412 | T/C | — | uncertain significance |
| rs762157400 | 12:63,061,084 | T/C | — | uncertain significance |
| rs778536082 | 12:63,083,517 | T/C | — | uncertain significance |
| rs199771693 | 12:63,083,583 | G/A | — | uncertain significance |
| rs61756417 | 12:63,087,765 | A/G | — | uncertain significance |
| rs200725314 | 12:63,113,958 | T/C | — | uncertain significance |
| rs778597878 | 12:63,114,033 | T/C | — | uncertain significance |
| rs376052127 | 12:63,131,301 | C/T | — | uncertain significance |
| rs2541523026 | 12:63,131,349 | T/C | — | uncertain significance |
| rs2029721 | 12:63,149,344 | G/A | coding sequence variant | — |
| rs189572423 | 12:63,152,963 | T/G | downstream gene variant | — |
| rs549433 | 12:63,180,816 | T/C | intron variant | — |
| rs943739059 | 12:63,182,054 | A/G | — | uncertain significance |
| rs377085423 | 12:63,182,109 | T/A | — | uncertain significance |
| rs528828146 | 12:63,187,673 | T/C | — | — |
| rs370030873 | 12:63,195,657 | T/A | — | uncertain significance |
| rs745843860 | 12:63,195,702 | C/A | — | uncertain significance |
| rs144982343 | 12:63,195,739 | T/G | — | benign |
| rs199959694 | 12:63,195,741 | C/T | — | uncertain significance |
| rs374889057 | 12:63,195,915 | T/C | — | uncertain significance |
| rs775923431 | 12:63,225,895 | G/A | — | uncertain significance |
| rs773011134 | 12:63,225,941 | G/A | — | uncertain significance |
| rs747489418 | 12:63,225,989 | T/C | — | uncertain significance |
| rs745962496 | 12:63,264,526 | G/A | — | — |
| rs699582 | 12:63,300,856 | G/A | intron variant | — |
| rs812814 | 12:63,303,767 | G/C | intron variant | — |
| rs772566 | 12:63,307,248 | T/C | intron variant | — |
| rs745460816 | 12:63,328,393 | C/G | — | uncertain significance |
| rs764950863 | 12:63,328,423 | C/T | — | uncertain significance |
| rs749669503 | 12:63,328,441 | C/T | — | uncertain significance |
| rs553231617 | 12:63,328,465 | C/G | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.