PPP1R15A
protein phosphatase 1 regulatory subunit 15A
Summary
This gene is a member of a group of genes whose transcript levels are increased following stressful growth arrest conditions and treatment with DNA-damaging agents. The induction of this gene by ionizing radiation occurs in certain cell lines regardless of p53 status, and its protein response is correlated with apoptosis following ionizing radiation. [provided by RefSeq, Jul 2008]
Known Variants57 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs192014448 | 19:49,373,695 | G/A | upstream gene variant | — |
| rs837608 | 19:49,374,541 | C/T | upstream gene variant | — |
| rs626974 | 19:49,375,900 | T/C | regulatory region variant | — |
| rs138534953 | 19:49,376,095 | G/C | regulatory region variant | — |
| rs552207545 | 19:49,376,497 | C/T | — | uncertain significance |
| rs1193016880 | 19:49,376,572 | C/T | — | likely benign |
| rs374067843 | 19:49,376,611 | C/T | — | uncertain significance |
| rs926658205 | 19:49,376,656 | G/A | — | uncertain significance |
| rs369203609 | 19:49,376,681 | C/T | — | uncertain significance |
| rs2037034197 | 19:49,376,684 | G/T | — | uncertain significance |
| rs1458358276 | 19:49,376,701 | C/T | — | uncertain significance |
| rs2037034595 | 19:49,376,708 | C/T | — | uncertain significance |
| rs374482307 | 19:49,376,875 | G/A | — | uncertain significance |
| rs150728200 | 19:49,376,897 | A/G | — | uncertain significance |
| rs137978264 | 19:49,376,905 | C/T | — | uncertain significance |
| rs548915056 | 19:49,376,920 | C/G | — | uncertain significance |
| rs199891815 | 19:49,376,992 | G/T | — | uncertain significance |
| rs367785147 | 19:49,376,999 | A/T | — | uncertain significance |
| rs77377218 | 19:49,377,042 | G/A | — | benign |
| rs2037040251 | 19:49,377,043 | G/C | — | uncertain significance |
| rs184379585 | 19:49,377,058 | G/A | — | uncertain significance |
| rs611251 | 19:49,377,086 | T/C | missense variant | — |
| rs2514343025 | 19:49,377,140 | C/T | — | uncertain significance |
| rs754378637 | 19:49,377,155 | C/G | — | likely benign |
| rs574085051 | 19:49,377,232 | G/A | — | uncertain significance |
| rs777713643 | 19:49,377,256 | G/A | — | likely benign |
| rs747248462 | 19:49,377,277 | C/T | — | likely benign |
| rs148913925 | 19:49,377,278 | G/A | — | uncertain significance |
| rs1298062765 | 19:49,377,371 | C/T | — | uncertain significance |
| rs2514343506 | 19:49,377,386 | T/C | — | uncertain significance |
| rs777970448 | 19:49,377,442 | G/A | — | uncertain significance |
| rs201957583 | 19:49,377,472 | T/C | — | uncertain significance |
| rs373762322 | 19:49,377,496 | A/G | — | uncertain significance |
| rs750340990 | 19:49,377,504 | C/G | — | uncertain significance |
| rs2037052297 | 19:49,377,653 | C/T | — | uncertain significance |
| rs372040847 | 19:49,377,746 | C/A | — | uncertain significance |
| rs535002242 | 19:49,377,748 | G/C | — | uncertain significance |
| rs140853052 | 19:49,377,781 | G/T | — | likely benign |
| rs144400267 | 19:49,377,793 | C/T | — | uncertain significance |
| rs769349958 | 19:49,377,816 | G/C | — | uncertain significance |
| rs34457521 | 19:49,378,095 | C/T | — | benign |
| rs1205118726 | 19:49,378,099 | C/T | — | uncertain significance |
| rs769169927 | 19:49,378,100 | G/A | — | likely benign |
| rs538712004 | 19:49,378,112 | C/T | — | uncertain significance |
| rs141370460 | 19:49,378,864 | C/T | — | benign |
| rs1009377941 | 19:49,378,910 | G/A | — | uncertain significance |
| rs538298636 | 19:49,378,964 | C/T | — | uncertain significance |
| rs556876971 | 19:49,378,965 | G/C | — | uncertain significance |
| rs761391876 | 19:49,378,968 | A/T | — | uncertain significance |
| rs764387649 | 19:49,378,977 | G/A | — | uncertain significance |
| rs147256383 | 19:49,378,988 | C/T | — | uncertain significance |
| rs144725427 | 19:49,378,998 | A/G | — | likely benign |
| rs2037075693 | 19:49,379,000 | G/A | — | uncertain significance |
| rs2514345615 | 19:49,379,012 | C/A | — | uncertain significance |
| rs2514345702 | 19:49,379,079 | C/A | — | uncertain significance |
| rs755786656 | 19:49,379,127 | C/G | — | uncertain significance |
| rs524 | 19:49,379,167 | C/T | synonymous variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.