PHLPP2
PH domain and leucine rich repeat protein phosphatase 2
Summary
Predicted to enable metal ion binding activity and phosphoprotein phosphatase activity. Predicted to be involved in intracellular signal transduction. Located in several cellular components, including cilium; intercellular bridge; and mitotic spindle. [provided by Alliance of Genome Resources, Apr 2025]
Known Variants90 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs201141453 | 16:71,682,803 | G/A | — | uncertain significance |
| rs747492423 | 16:71,682,896 | T/A | — | uncertain significance |
| rs149705576 | 16:71,682,911 | T/C | — | likely benign |
| rs2044673909 | 16:71,682,912 | G/T | — | uncertain significance |
| rs780842467 | 16:71,682,917 | A/G | — | uncertain significance |
| rs929847519 | 16:71,683,218 | G/A | — | uncertain significance |
| rs2507769349 | 16:71,683,244 | C/A | — | uncertain significance |
| rs140495800 | 16:71,683,293 | C/T | — | uncertain significance |
| rs776304023 | 16:71,683,317 | C/G | — | uncertain significance |
| rs551193903 | 16:71,683,329 | C/T | — | uncertain significance |
| rs577337641 | 16:71,683,339 | C/A | — | uncertain significance |
| rs199811510 | 16:71,683,349 | G/C | — | likely benign |
| rs1298512448 | 16:71,683,391 | G/T | — | uncertain significance |
| rs368469959 | 16:71,683,398 | T/G | — | uncertain significance |
| rs149141921 | 16:71,683,418 | C/T | — | uncertain significance |
| rs780819572 | 16:71,683,430 | G/A | — | uncertain significance |
| rs757783945 | 16:71,683,500 | C/A | — | uncertain significance |
| rs2044680971 | 16:71,683,547 | C/T | — | uncertain significance |
| rs1423921848 | 16:71,683,593 | T/C | — | uncertain significance |
| rs765346195 | 16:71,683,605 | C/T | — | uncertain significance |
| rs768901557 | 16:71,683,706 | T/C | — | uncertain significance |
| rs142287063 | 16:71,683,759 | G/A | — | benign |
| rs368274198 | 16:71,683,830 | A/T | — | uncertain significance |
| rs757987779 | 16:71,683,850 | G/A | — | uncertain significance |
| rs142472702 | 16:71,686,790 | C/T | — | uncertain significance |
| rs61733128 | 16:71,686,811 | G/A | — | uncertain significance |
| rs765294354 | 16:71,686,856 | G/T | — | uncertain significance |
| rs569703138 | 16:71,686,866 | G/C | — | uncertain significance |
| rs139087912 | 16:71,686,904 | T/C | — | uncertain significance |
| rs758916211 | 16:71,689,147 | G/C | — | uncertain significance |
| rs759756307 | 16:71,689,227 | G/A | — | uncertain significance |
| rs753079089 | 16:71,689,242 | C/T | — | uncertain significance |
| rs752054132 | 16:71,689,260 | C/T | — | uncertain significance |
| rs2507784680 | 16:71,689,269 | T/A | — | uncertain significance |
| rs1200461372 | 16:71,689,304 | A/C | — | uncertain significance |
| rs780122420 | 16:71,690,543 | G/C | — | uncertain significance |
| rs12051443 | 16:71,691,329 | G/A | intron variant | — |
| rs536324202 | 16:71,692,667 | C/A | — | uncertain significance |
| rs144818546 | 16:71,693,773 | C/G | intron variant | — |
| rs144725655 | 16:71,697,889 | G/A | — | uncertain significance |
| rs751061799 | 16:71,697,953 | C/T | — | uncertain significance |
| rs750166651 | 16:71,697,961 | A/G | — | uncertain significance |
| rs140410920 | 16:71,697,964 | G/A | — | uncertain significance |
| rs745898023 | 16:71,701,117 | G/A | — | uncertain significance |
| rs1262419143 | 16:71,703,251 | C/T | — | uncertain significance |
| rs113061734 | 16:71,703,264 | T/C | — | likely benign |
| rs12924631 | 16:71,705,774 | G/A | intron variant | — |
| rs778481434 | 16:71,706,174 | T/C | — | uncertain significance |
| rs1330988419 | 16:71,706,180 | A/G | — | likely benign |
| rs968349190 | 16:71,710,373 | C/T | — | uncertain significance |
| rs377712192 | 16:71,710,374 | G/A | — | uncertain significance |
| rs148584091 | 16:71,710,408 | C/G | — | likely benign |
| rs550837888 | 16:71,710,463 | T/C | — | uncertain significance |
| rs2044970678 | 16:71,712,715 | T/C | — | uncertain significance |
| rs1018484160 | 16:71,712,779 | T/C | — | uncertain significance |
| rs749630797 | 16:71,712,815 | A/G | — | uncertain significance |
| rs1333557875 | 16:71,712,827 | G/C | — | uncertain significance |
| rs1251019088 | 16:71,712,863 | T/C | — | uncertain significance |
| rs755192177 | 16:71,713,323 | C/G | — | uncertain significance |
| rs371147545 | 16:71,713,346 | T/C | — | uncertain significance |
| rs145216542 | 16:71,713,348 | G/A | — | likely benign |
| rs148901878 | 16:71,713,383 | T/C | — | likely benign |
| rs1485044334 | 16:71,713,407 | G/A | — | uncertain significance |
| rs774406482 | 16:71,715,717 | T/C | — | uncertain significance |
| rs778674012 | 16:71,715,764 | G/C | — | uncertain significance |
| rs113166271 | 16:71,715,768 | T/C | — | uncertain significance |
| rs2479340612 | 16:71,715,771 | C/A | — | uncertain significance |
| rs189946562 | 16:71,718,392 | C/T | — | uncertain significance |
| rs996692240 | 16:71,718,447 | C/G | — | uncertain significance |
| rs750142984 | 16:71,718,464 | C/G | — | uncertain significance |
| rs144641434 | 16:71,718,504 | T/C | — | likely benign |
| rs78064607 | 16:71,723,181 | C/T | intron variant | — |
| rs764178203 | 16:71,724,438 | G/A | — | uncertain significance |
| rs369156314 | 16:71,724,485 | G/C | — | uncertain significance |
| rs2543450240 | 16:71,736,524 | C/G | — | uncertain significance |
| rs374229954 | 16:71,736,558 | G/A | — | uncertain significance |
| rs76788735 | 16:71,743,169 | T/C | regulatory region variant | — |
| rs7203216 | 16:71,745,518 | C/G | — | — |
| rs762340387 | 16:71,748,434 | G/C | — | uncertain significance |
| rs558239578 | 16:71,748,481 | G/A | — | uncertain significance |
| rs576309937 | 16:71,748,482 | C/A | — | uncertain significance |
| rs762217683 | 16:71,748,510 | A/T | — | uncertain significance |
| rs1262948974 | 16:71,748,515 | A/T | — | uncertain significance |
| rs765932644 | 16:71,748,520 | G/A | — | uncertain significance |
| rs2543465402 | 16:71,748,529 | G/A | — | uncertain significance |
| rs137910373 | 16:71,748,544 | G/C | — | uncertain significance |
| rs2543465451 | 16:71,748,547 | G/A | — | uncertain significance |
| rs773396475 | 16:71,748,592 | T/C | — | uncertain significance |
| rs192480876 | 16:71,748,677 | T/G | — | uncertain significance |
| rs746313254 | 16:71,748,692 | G/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.