SMG8
SMG8 nonsense mediated mRNA decay factor
Summary
Involved in nuclear-transcribed mRNA catabolic process, nonsense-mediated decay and regulation of protein kinase activity. Predicted to be located in cytosol. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants55 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs368076111 | 17:57,287,420 | G/C | — | uncertain significance |
| rs142656435 | 17:57,287,425 | G/A | — | uncertain significance |
| rs200954396 | 17:57,287,453 | C/T | — | uncertain significance |
| rs6503905 | 17:57,287,454 | A/G | synonymous variant | — |
| rs186725683 | 17:57,287,482 | G/A | — | uncertain significance |
| rs148984334 | 17:57,287,586 | A/G | — | likely benign |
| rs2546572792 | 17:57,287,591 | T/C | — | uncertain significance |
| rs755948975 | 17:57,287,697 | G/A | — | likely benign |
| rs759055595 | 17:57,287,762 | G/C | — | uncertain significance |
| rs145809144 | 17:57,287,820 | C/A | — | uncertain significance |
| rs62081948 | 17:57,287,844 | G/A | — | likely benign |
| rs780141766 | 17:57,288,021 | A/C | — | likely benign |
| rs2147863904 | 17:57,288,035 | A/G | — | pathogenic |
| rs146018691 | 17:57,288,044 | T/C | — | uncertain significance |
| rs751678341 | 17:57,288,055 | C/A | — | uncertain significance |
| rs1460427478 | 17:57,288,092 | T/G | — | uncertain significance |
| rs1169670381 | 17:57,288,093 | C/G | — | uncertain significance |
| rs201168751 | 17:57,288,160 | G/C | — | uncertain significance |
| rs199713610 | 17:57,288,269 | C/G | — | uncertain significance |
| rs2492132571 | 17:57,288,427 | G/A | — | uncertain significance |
| rs201593126 | 17:57,288,469 | G/C | — | uncertain significance |
| rs148740401 | 17:57,288,479 | G/A | — | uncertain significance |
| rs2046944212 | 17:57,288,545 | G/A | — | uncertain significance |
| rs1009945043 | 17:57,288,567 | C/G | — | uncertain significance |
| rs116637376 | 17:57,288,569 | G/A | — | benign |
| rs2546573515 | 17:57,288,619 | G/T | — | uncertain significance |
| rs1284983542 | 17:57,288,671 | T/C | — | uncertain significance |
| rs756739941 | 17:57,288,749 | A/T | — | uncertain significance |
| rs1304702168 | 17:57,288,763 | G/C | — | uncertain significance |
| rs1365715610 | 17:57,288,823 | A/G | — | uncertain significance |
| rs2546573668 | 17:57,288,851 | G/A | — | uncertain significance |
| rs2546573765 | 17:57,289,005 | T/C | — | likely benign |
| rs2046946295 | 17:57,289,010 | G/A | — | uncertain significance |
| rs2546573781 | 17:57,289,043 | T/C | — | uncertain significance |
| rs747387982 | 17:57,289,709 | A/C | — | uncertain significance |
| rs777293335 | 17:57,289,711 | C/A | — | uncertain significance |
| rs143473864 | 17:57,289,730 | G/T | — | benign |
| rs142548382 | 17:57,289,805 | T/A | — | likely benign |
| rs2546574278 | 17:57,290,159 | G/C | — | uncertain significance |
| rs1188689328 | 17:57,290,234 | C/T | — | uncertain significance |
| rs201032698 | 17:57,290,328 | C/T | — | uncertain significance |
| rs771233208 | 17:57,290,333 | G/A | — | uncertain significance |
| rs549130197 | 17:57,290,393 | G/A | — | likely benign |
| rs146340466 | 17:57,290,502 | C/T | — | benign |
| rs2546574446 | 17:57,290,520 | T/C | — | uncertain significance |
| rs2546574489 | 17:57,290,619 | T/G | — | pathogenic |
| rs151326790 | 17:57,290,667 | G/A | — | uncertain significance |
| rs755161625 | 17:57,290,699 | C/T | — | pathogenic |
| rs2546574596 | 17:57,290,847 | C/T | — | uncertain significance |
| rs376663010 | 17:57,290,907 | T/C | — | uncertain significance |
| rs2546574647 | 17:57,290,913 | T/G | — | uncertain significance |
| rs2546574662 | 17:57,290,933 | G/T | — | uncertain significance |
| rs2546575083 | 17:57,292,156 | T/A | — | uncertain significance |
| rs138640712 | 17:57,292,192 | G/A | — | likely benign |
| rs372496724 | 17:57,292,364 | G/T | — | likely benign |
Gene information from NCBI Gene. Variant classifications from ClinVar.