PPP4R3B
protein phosphatase 4 regulatory subunit 3B
Summary
Predicted to enable protein phosphatase activator activity. Involved in regulation of double-strand break repair. Located in centrosome; chromatin; and nuclear speck. Part of protein phosphatase 4 complex. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants34 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1058582 | 2:55,775,069 | C/A | — | — |
| rs2528413169 | 2:55,777,055 | C/A | — | uncertain significance |
| rs750842062 | 2:55,777,061 | G/A | — | uncertain significance |
| rs1685059476 | 2:55,777,107 | A/C | — | uncertain significance |
| rs2528415170 | 2:55,777,117 | T/A | — | uncertain significance |
| rs1275372545 | 2:55,785,913 | T/G | — | uncertain significance |
| rs2528528462 | 2:55,785,924 | A/C | — | uncertain significance |
| rs1311085300 | 2:55,785,958 | A/T | — | uncertain significance |
| rs1339749536 | 2:55,786,011 | C/T | — | uncertain significance |
| rs571012588 | 2:55,786,023 | C/T | — | uncertain significance |
| rs373358664 | 2:55,786,031 | G/C | — | uncertain significance |
| rs751807506 | 2:55,791,526 | A/G | — | uncertain significance |
| rs1403349605 | 2:55,791,592 | G/C | — | uncertain significance |
| rs370066372 | 2:55,792,155 | G/A | — | uncertain significance |
| rs150589498 | 2:55,792,158 | G/A | — | uncertain significance |
| rs780436419 | 2:55,800,839 | G/A | — | uncertain significance |
| rs1006605817 | 2:55,800,859 | C/T | — | uncertain significance |
| rs1975484 | 2:55,803,167 | T/A | intron variant | — |
| rs376675177 | 2:55,804,460 | T/C | — | uncertain significance |
| rs2528915912 | 2:55,808,773 | C/T | — | uncertain significance |
| rs2528969983 | 2:55,812,216 | C/T | — | uncertain significance |
| rs139317897 | 2:55,812,278 | G/A | — | uncertain significance |
| rs752226272 | 2:55,813,756 | T/A | — | uncertain significance |
| rs905688298 | 2:55,816,050 | C/G | — | uncertain significance |
| rs35178059 | 2:55,825,577 | T/C | — | uncertain significance |
| rs1692126816 | 2:55,825,762 | T/G | — | uncertain significance |
| rs143951318 | 2:55,826,001 | G/C | — | uncertain significance |
| rs758451580 | 2:55,826,111 | C/T | — | uncertain significance |
| rs147747743 | 2:55,826,163 | C/G | — | uncertain significance |
| rs2586970 | 2:55,829,967 | A/G | intron variant | — |
| rs782590 | 2:55,843,413 | C/T | upstream gene variant | — |
| rs199629271 | 2:55,844,316 | T/C | — | uncertain significance |
| rs2529398237 | 2:55,844,415 | C/G | — | uncertain significance |
| rs10200159 | 2:55,845,109 | T/C | coding sequence variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.