MPG
N-methylpurine DNA glycosylase
Summary
Enables DNA binding activity. Predicted to be involved in base-excision repair. Located in cytosol and nucleoplasm. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants43 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs3176364 | 16:127,577 | G/T | — | — |
| rs371060262 | 16:128,260 | G/T | — | — |
| rs710079 | 16:129,223 | C/T | regulatory region variant | — |
| rs572798244 | 16:129,428 | G/T | — | uncertain significance |
| rs2542772270 | 16:129,458 | C/T | — | likely benign |
| rs2266605 | 16:129,492 | C/T | — | benign |
| rs2266606 | 16:129,588 | G/A | — | benign |
| rs2542772970 | 16:129,601 | A/G | — | uncertain significance |
| rs376049637 | 16:129,638 | G/A | — | uncertain significance |
| rs985687646 | 16:129,646 | T/A | — | uncertain significance |
| rs1307996142 | 16:129,686 | C/A | — | uncertain significance |
| rs2858056 | 16:130,893 | G/C | upstream gene variant | — |
| rs2541632 | 16:131,109 | C/T | upstream gene variant | — |
| rs184069239 | 16:132,752 | A/T | regulatory region variant | — |
| rs3176416 | 16:132,850 | G/A | downstream gene variant | — |
| rs144044199 | 16:133,061 | G/A | — | uncertain significance |
| rs1376675397 | 16:133,096 | A/G | — | uncertain significance |
| rs146178270 | 16:133,099 | G/A | — | uncertain significance |
| rs774617942 | 16:133,117 | C/A | — | uncertain significance |
| rs1898298344 | 16:133,120 | G/T | — | uncertain significance |
| rs2542779234 | 16:133,127 | A/G | — | uncertain significance |
| rs775633395 | 16:133,220 | A/G | — | uncertain significance |
| rs149812218 | 16:133,222 | G/A | — | uncertain significance |
| rs2542779604 | 16:133,238 | T/C | — | uncertain significance |
| rs3176428 | 16:134,476 | G/A | regulatory region variant | — |
| rs1567126045 | 16:135,400 | G/C | — | uncertain significance |
| rs200919197 | 16:135,480 | C/G | — | uncertain significance |
| rs147661014 | 16:135,492 | G/A | — | uncertain significance |
| rs762883064 | 16:135,507 | A/G | — | uncertain significance |
| rs766487967 | 16:135,516 | G/A | — | uncertain significance |
| rs577355454 | 16:135,535 | C/G | — | uncertain significance |
| rs866593837 | 16:135,582 | G/A | — | uncertain significance |
| rs1567126349 | 16:135,591 | C/A | — | uncertain significance |
| rs202204500 | 16:135,608 | G/T | — | uncertain significance |
| rs1311472407 | 16:135,615 | C/T | — | uncertain significance |
| rs2542786290 | 16:135,658 | C/T | — | uncertain significance |
| rs150131864 | 16:135,660 | C/T | — | uncertain significance |
| rs974375687 | 16:135,672 | G/A | — | uncertain significance |
| rs969785856 | 16:135,693 | C/T | — | uncertain significance |
| rs528566515 | 16:135,700 | C/T | — | uncertain significance |
| rs149318391 | 16:135,706 | G/A | — | uncertain significance |
| rs768002164 | 16:135,732 | G/A | — | uncertain significance |
| rs1174113763 | 16:135,741 | G/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.