ENDOG
endonuclease G
Summary
The protein encoded by this gene is a nuclear encoded endonuclease that is localized in the mitochondrion. The encoded protein is widely distributed among animals and cleaves DNA at GC tracts. This protein is capable of generating the RNA primers required by DNA polymerase gamma to initiate replication of mitochondrial DNA. [provided by RefSeq, Jul 2008]
Known Variants25 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs10988130 | 9:131,579,579 | A/G | upstream gene variant | — |
| rs2490911080 | 9:131,581,013 | G/T | — | uncertain significance |
| rs1327013077 | 9:131,581,087 | G/C | — | uncertain significance |
| rs2490911745 | 9:131,581,150 | G/A | — | uncertain significance |
| rs757963132 | 9:131,581,173 | G/C | — | likely benign |
| rs777462203 | 9:131,581,204 | T/G | — | uncertain significance |
| rs746520947 | 9:131,581,226 | G/T | — | uncertain significance |
| rs542727367 | 9:131,581,264 | C/T | — | uncertain significance |
| rs970057720 | 9:131,581,292 | G/C | — | uncertain significance |
| rs762857548 | 9:131,581,312 | G/C | — | uncertain significance |
| rs2490912841 | 9:131,581,352 | C/T | — | uncertain significance |
| rs2490918735 | 9:131,583,027 | C/T | — | uncertain significance |
| rs528071859 | 9:131,583,052 | T/C | — | uncertain significance |
| rs547914635 | 9:131,583,066 | C/T | — | uncertain significance |
| rs556705072 | 9:131,583,093 | G/A | — | uncertain significance |
| rs2490924967 | 9:131,584,643 | G/C | — | uncertain significance |
| rs55985529 | 9:131,584,649 | C/T | — | benign |
| rs369635561 | 9:131,584,723 | A/G | — | uncertain significance |
| rs61737988 | 9:131,584,729 | G/T | — | benign |
| rs61737987 | 9:131,584,732 | C/T | — | benign |
| rs2490925430 | 9:131,584,752 | C/T | — | uncertain significance |
| rs755497118 | 9:131,584,779 | C/T | — | uncertain significance |
| rs142344729 | 9:131,584,780 | G/A | — | uncertain significance |
| rs371060113 | 9:131,584,816 | C/T | — | uncertain significance |
| rs750255865 | 9:131,584,849 | G/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.