MRAS
muscle RAS oncogene homolog
Summary
This gene encodes a member of the Ras family of small GTPases. These membrane-associated proteins function as signal transducers in multiple processes including cell growth and differentiation, and dysregulation of Ras signaling has been associated with many types of cancer. The encoded protein may play a role in the tumor necrosis factor-alpha and MAP kinase signaling pathways. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Nov 2011]
Known Variants195 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs3755751 | 3:138,065,567 | A/C | — | — |
| rs11713141 | 3:138,067,626 | C/T | regulatory region variant | — |
| rs1199337 | 3:138,088,064 | G/C | intron variant | — |
| rs7626388 | 3:138,089,038 | G/A | intron variant | — |
| rs1199333 | 3:138,091,701 | G/T | splice region variant | benign |
| rs368097379 | 3:138,091,719 | G/A | — | uncertain significance |
| rs35056274 | 3:138,091,737 | C/T | — | likely benign |
| rs767548259 | 3:138,091,738 | G/A | — | uncertain significance |
| rs752887551 | 3:138,091,740 | C/T | — | likely benign |
| rs778102030 | 3:138,091,741 | G/A | — | uncertain significance |
| rs547745521 | 3:138,091,747 | A/G | — | conflicting classifications of pathogenicity |
| rs2474071974 | 3:138,091,748 | G/C | — | uncertain significance |
| rs2474071987 | 3:138,091,752 | C/A | — | uncertain significance |
| rs757673646 | 3:138,091,754 | A/G | — | uncertain significance |
| rs2474072019 | 3:138,091,755 | C/T | — | likely benign |
| rs2054705350 | 3:138,091,757 | T/C | — | uncertain significance |
| rs2474072054 | 3:138,091,761 | C/T | — | likely benign |
| rs2474072068 | 3:138,091,763 | C/T | — | uncertain significance |
| rs779084199 | 3:138,091,764 | A/G | — | likely benign |
| rs746403874 | 3:138,091,767 | C/T | — | likely benign |
| rs2054705647 | 3:138,091,770 | G/A | — | likely benign |
| rs1239516898 | 3:138,091,782 | G/A | — | likely benign |
| rs142535762 | 3:138,091,791 | G/T | — | likely benign |
| rs1560171992 | 3:138,091,792 | G/C | — | likely pathogenic |
| rs1576359216 | 3:138,091,793 | G/T | — | likely pathogenic |
| rs2054706404 | 3:138,091,805 | G/C | — | uncertain significance |
| rs760022997 | 3:138,091,809 | C/A | — | likely benign |
| rs2474072369 | 3:138,091,810 | C/T | — | uncertain significance |
| rs747697719 | 3:138,091,839 | T/C | — | likely benign |
| rs2474072483 | 3:138,091,845 | T/G | — | likely benign |
| rs2474072512 | 3:138,091,855 | C/T | — | uncertain significance |
| rs1321282194 | 3:138,091,863 | T/C | — | likely benign |
| rs1198226723 | 3:138,091,884 | T/C | — | likely benign |
| rs2054707593 | 3:138,091,886 | C/T | — | uncertain significance |
| rs954888797 | 3:138,091,887 | G/A | — | likely benign |
| rs2474072674 | 3:138,091,890 | G/C | — | uncertain significance |
| rs762443438 | 3:138,091,896 | C/T | — | likely benign |
| rs2474072709 | 3:138,091,898 | A/G | — | uncertain significance |
| rs16848033 | 3:138,091,902 | A/G | — | benign |
| rs1157596507 | 3:138,091,906 | G/A | — | uncertain significance |
| rs774071033 | 3:138,091,907 | C/T | — | uncertain significance |
| rs2474072764 | 3:138,091,909 | A/G | — | uncertain significance |
| rs2054708327 | 3:138,091,914 | G/A | — | likely benign |
| rs373753637 | 3:138,091,917 | C/T | — | conflicting classifications of pathogenicity |
| rs201232759 | 3:138,091,926 | C/G | — | likely benign |
| rs57184972 | 3:138,092,028 | G/A | — | benign |
| rs185244 | 3:138,092,889 | C/T | intron variant | — |
| rs194146 | 3:138,092,906 | A/C | — | — |
| rs183151 | 3:138,092,950 | A/G | intron variant | — |
| rs1678443 | 3:138,097,534 | C/A | intron variant | — |
| rs1679147 | 3:138,097,537 | A/G | intron variant | — |
| rs1308362 | 3:138,103,927 | A/T | regulatory region variant | — |
| rs71310214 | 3:138,104,027 | A/T | — | — |
| rs34905952 | 3:138,104,635 | G/A | intron variant | — |
| rs1720825 | 3:138,108,083 | A/T | — | — |
| rs9848655 | 3:138,108,352 | G/A | intron variant | — |
| rs9864898 | 3:138,111,751 | C/T | intron variant | — |
| rs1199328 | 3:138,112,107 | G/C | — | — |
| rs1427542358 | 3:138,116,150 | C/T | — | likely benign |
| rs1190844251 | 3:138,116,156 | C/T | — | likely benign |
| rs753926542 | 3:138,116,161 | C/T | — | likely benign |
| rs761952196 | 3:138,116,168 | C/G | — | uncertain significance |
| rs2055258576 | 3:138,116,169 | T/A | — | uncertain significance |
| rs1576387876 | 3:138,116,175 | C/T | — | likely pathogenic |
| rs2108561531 | 3:138,116,180 | G/C | — | uncertain significance |
| rs1576387885 | 3:138,116,184 | A/G | — | likely pathogenic |
| rs563066079 | 3:138,116,197 | C/T | — | likely benign |
| rs752073267 | 3:138,116,204 | C/T | — | uncertain significance |
| rs2474152740 | 3:138,116,220 | G/A | — | uncertain significance |
| rs756765006 | 3:138,116,223 | C/T | — | uncertain significance |
| rs373727168 | 3:138,116,224 | G/A | — | likely benign |
| rs1263213336 | 3:138,116,227 | G/A | — | likely benign |
| rs2055260500 | 3:138,116,233 | C/T | — | likely benign |
| rs745474939 | 3:138,116,239 | C/T | — | likely benign |
| rs576537185 | 3:138,116,242 | C/T | — | likely benign |
| rs2055260842 | 3:138,116,243 | G/A | — | uncertain significance |
| rs775370867 | 3:138,116,247 | A/C | — | uncertain significance |
| rs920136386 | 3:138,116,248 | C/T | — | likely benign |
| rs746791585 | 3:138,116,251 | C/T | — | likely benign |
| rs2474152921 | 3:138,116,254 | C/T | — | likely benign |
| rs776600463 | 3:138,116,257 | T/C | — | likely benign |
| rs548156011 | 3:138,116,263 | G/A | — | likely benign |
| rs2474152970 | 3:138,116,264 | G/A | — | uncertain significance |
| rs2055261626 | 3:138,116,265 | C/A | — | uncertain significance |
| rs1453377231 | 3:138,116,272 | T/A | — | uncertain significance |
| rs2055261939 | 3:138,116,277 | A/G | — | uncertain significance |
| rs138905383 | 3:138,116,278 | C/T | — | likely benign |
| rs1307344253 | 3:138,116,279 | G/A | — | uncertain significance |
| rs1053419617 | 3:138,116,285 | C/T | — | uncertain significance |
| rs2055262544 | 3:138,116,286 | G/A | — | uncertain significance |
| rs755337901 | 3:138,116,296 | G/A | — | likely benign |
| rs151130678 | 3:138,116,302 | C/T | — | likely benign |
| rs1301422225 | 3:138,116,303 | C/T | — | likely benign |
| rs372879145 | 3:138,116,304 | T/G | — | uncertain significance |
| rs2474153179 | 3:138,116,306 | C/T | — | uncertain significance |
| rs2474153196 | 3:138,116,307 | G/A | — | uncertain significance |
| rs139032711 | 3:138,116,308 | C/A | — | likely benign |
| rs2474153224 | 3:138,116,309 | G/A | — | uncertain significance |
| rs200375034 | 3:138,116,322 | G/A | — | uncertain significance |
| rs1447536745 | 3:138,116,323 | A/G | — | uncertain significance |
Showing 100 of 195 variants. Use the SNP search for the full list.
Gene information from NCBI Gene. Variant classifications from ClinVar.