SMG5
SMG5 nonsense mediated mRNA decay factor
Summary
SMG5 is involved in nonsense-mediated mRNA decay (Ohnishi et al., 2003 [PubMed 14636577]).[supplied by OMIM, Mar 2008]
Known Variants68 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs11264461 | 1:156,218,642 | A/G | upstream gene variant | — |
| rs148949638 | 1:156,220,455 | G/C | — | uncertain significance |
| rs147716722 | 1:156,220,659 | C/A | — | uncertain significance |
| rs751882204 | 1:156,220,668 | A/G | — | likely benign |
| rs1252532672 | 1:156,220,719 | G/A | — | uncertain significance |
| rs1466728270 | 1:156,220,747 | G/C | — | uncertain significance |
| rs368650396 | 1:156,220,755 | T/G | — | uncertain significance |
| rs2524949340 | 1:156,220,783 | G/A | — | uncertain significance |
| rs1558231002 | 1:156,221,224 | T/G | — | uncertain significance |
| rs776471889 | 1:156,221,236 | C/T | — | uncertain significance |
| rs368990362 | 1:156,221,254 | T/C | — | uncertain significance |
| rs1208843091 | 1:156,222,292 | A/G | — | uncertain significance |
| rs551786600 | 1:156,222,844 | C/T | — | uncertain significance |
| rs12024813 | 1:156,224,529 | C/A | intron variant | — |
| rs148723389 | 1:156,228,878 | T/C | — | likely benign |
| rs759492937 | 1:156,228,905 | C/T | — | uncertain significance |
| rs1481404533 | 1:156,228,930 | G/A | — | uncertain significance |
| rs755626951 | 1:156,230,250 | A/C | — | uncertain significance |
| rs2273833 | 1:156,233,189 | C/T | synonymous variant | — |
| rs550868260 | 1:156,233,209 | C/T | — | uncertain significance |
| rs370569638 | 1:156,233,220 | C/T | — | uncertain significance |
| rs773737710 | 1:156,233,221 | G/A | — | uncertain significance |
| rs761614813 | 1:156,233,316 | C/T | — | uncertain significance |
| rs2525004708 | 1:156,233,331 | C/A | — | uncertain significance |
| rs7512751 | 1:156,234,439 | T/C | — | — |
| rs142511385 | 1:156,234,673 | C/T | intron variant | — |
| rs12118238 | 1:156,235,221 | G/A | intron variant | — |
| rs2525017466 | 1:156,235,583 | G/A | — | uncertain significance |
| rs1558238397 | 1:156,235,593 | C/T | — | uncertain significance |
| rs528845513 | 1:156,235,625 | G/A | — | likely benign |
| rs145457977 | 1:156,235,635 | G/A | — | uncertain significance |
| rs776780601 | 1:156,235,707 | T/A | — | uncertain significance |
| rs751930695 | 1:156,235,730 | T/C | — | uncertain significance |
| rs570233291 | 1:156,235,773 | G/A | — | uncertain significance |
| rs34377219 | 1:156,235,800 | G/A | — | benign |
| rs567751929 | 1:156,235,806 | G/A | — | uncertain significance |
| rs1558238825 | 1:156,235,836 | C/T | — | uncertain significance |
| rs137951764 | 1:156,235,857 | C/T | — | uncertain significance |
| rs1662123683 | 1:156,235,950 | A/G | — | uncertain significance |
| rs777121152 | 1:156,236,043 | G/A | — | uncertain significance |
| rs376314067 | 1:156,236,049 | G/A | — | uncertain significance |
| rs575799058 | 1:156,236,111 | G/A | — | uncertain significance |
| rs571601288 | 1:156,236,171 | T/C | — | uncertain significance |
| rs2525022823 | 1:156,236,340 | T/C | — | uncertain significance |
| rs1426492770 | 1:156,236,365 | T/C | — | uncertain significance |
| rs1662158092 | 1:156,236,371 | C/T | — | uncertain significance |
| rs2525023509 | 1:156,236,445 | A/G | — | uncertain significance |
| rs1314631334 | 1:156,237,264 | C/T | — | uncertain significance |
| rs2525027795 | 1:156,237,293 | C/T | — | uncertain significance |
| rs1558239969 | 1:156,237,300 | T/C | — | uncertain significance |
| rs571418441 | 1:156,237,306 | T/C | — | uncertain significance |
| rs2525027917 | 1:156,237,308 | T/C | — | uncertain significance |
| rs1012649128 | 1:156,237,371 | G/T | — | uncertain significance |
| rs143713625 | 1:156,237,377 | C/G | — | uncertain significance |
| rs750746992 | 1:156,237,392 | G/A | — | uncertain significance |
| rs1662213306 | 1:156,237,446 | G/A | — | uncertain significance |
| rs376736804 | 1:156,237,465 | C/T | — | likely benign |
| rs144344500 | 1:156,238,211 | A/G | — | benign |
| rs141888329 | 1:156,247,019 | C/T | — | uncertain significance |
| rs142253945 | 1:156,247,757 | C/T | — | uncertain significance |
| rs770015202 | 1:156,247,823 | C/T | — | uncertain significance |
| rs1662809846 | 1:156,248,752 | G/A | — | uncertain significance |
| rs147617947 | 1:156,248,802 | C/T | — | uncertain significance |
| rs769639682 | 1:156,252,413 | G/A | — | uncertain significance |
| rs1328590253 | 1:156,252,455 | G/A | — | uncertain significance |
| rs200968265 | 1:156,252,461 | C/A | — | uncertain significance |
| rs6684514 | 1:156,255,456 | G/A | missense variant | — |
| rs2104404 | 1:156,256,913 | C/A | downstream gene variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.