MCC
MCC regulator of Wnt signaling pathway
Summary
This gene is a candidate colorectal tumor suppressor gene that is thought to negatively regulate cell cycle progression. The orthologous gene in the mouse expresses a phosphoprotein associated with the plasma membrane and membrane organelles, and overexpression of the mouse protein inhibits entry into S phase. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]
Known Variants122 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs764906819 | 5:112,363,022 | G/T | — | uncertain significance |
| rs201704236 | 5:112,363,057 | C/T | — | uncertain significance |
| rs1028116706 | 5:112,363,093 | T/C | — | uncertain significance |
| rs386352328 | 5:112,363,108 | A/G | — | uncertain significance |
| rs2479534339 | 5:112,363,123 | T/C | — | uncertain significance |
| rs139859351 | 5:112,364,656 | C/T | — | uncertain significance |
| rs17313892 | 5:112,364,689 | T/A | — | benign |
| rs1231187860 | 5:112,364,698 | T/C | — | uncertain significance |
| rs1015638829 | 5:112,364,709 | A/G | — | uncertain significance |
| rs151182874 | 5:112,364,715 | C/T | — | uncertain significance |
| rs139210825 | 5:112,364,719 | C/G | — | uncertain significance |
| rs773046677 | 5:112,364,724 | T/C | — | uncertain significance |
| rs4705752 | 5:112,366,678 | A/G | intron variant | — |
| rs145075958 | 5:112,379,230 | C/T | — | uncertain significance |
| rs201477405 | 5:112,379,238 | G/A | — | likely benign |
| rs2479594502 | 5:112,379,246 | A/G | — | uncertain significance |
| rs1751869618 | 5:112,379,252 | C/A | — | uncertain significance |
| rs1445903770 | 5:112,379,267 | C/T | — | uncertain significance |
| rs2479594730 | 5:112,379,282 | T/A | — | uncertain significance |
| rs2479594734 | 5:112,379,284 | A/C | — | uncertain significance |
| rs777743671 | 5:112,379,288 | C/T | — | uncertain significance |
| rs2227948 | 5:112,379,289 | G/A | synonymous variant | — |
| rs121917731 | 5:112,379,320 | G/A | missense variant | pathogenic |
| rs6877570 | 5:112,380,723 | C/T | — | — |
| rs4073359 | 5:112,382,159 | G/A | intron variant | — |
| rs200797844 | 5:112,384,791 | T/A | — | uncertain significance |
| rs150279109 | 5:112,384,917 | C/T | — | uncertain significance |
| rs751790153 | 5:112,384,920 | G/A | — | uncertain significance |
| rs780543701 | 5:112,384,941 | G/T | — | uncertain significance |
| rs758707911 | 5:112,389,445 | T/G | — | uncertain significance |
| rs778137782 | 5:112,389,454 | C/T | — | uncertain significance |
| rs116597487 | 5:112,389,455 | G/A | — | benign |
| rs543836683 | 5:112,389,603 | T/C | — | likely benign |
| rs752109718 | 5:112,389,604 | C/T | — | uncertain significance |
| rs368313454 | 5:112,389,605 | G/A | — | likely benign |
| rs779662197 | 5:112,389,622 | C/T | — | uncertain significance |
| rs756995567 | 5:112,399,696 | G/A | — | uncertain significance |
| rs374053773 | 5:112,399,736 | C/T | — | uncertain significance |
| rs531626238 | 5:112,399,738 | G/A | — | uncertain significance |
| rs151039584 | 5:112,399,751 | C/G | — | likely benign |
| rs121917732 | 5:112,399,807 | C/T | missense variant | pathogenic |
| rs149204864 | 5:112,399,822 | C/A | — | uncertain significance |
| rs140691479 | 5:112,403,799 | C/T | — | likely benign |
| rs374240917 | 5:112,403,810 | G/T | — | uncertain significance |
| rs777351696 | 5:112,403,851 | A/T | — | uncertain significance |
| rs773355443 | 5:112,403,879 | C/T | — | uncertain significance |
| rs2479697684 | 5:112,406,807 | G/T | — | uncertain significance |
| rs35555142 | 5:112,406,814 | C/T | — | likely benign |
| rs1479813790 | 5:112,406,869 | C/T | — | uncertain significance |
| rs147427484 | 5:112,406,905 | T/A | — | uncertain significance |
| rs62373350 | 5:112,406,928 | C/A | — | likely benign |
| rs61263890 | 5:112,406,935 | C/A | — | benign |
| rs142795218 | 5:112,418,603 | C/T | — | uncertain significance |
| rs1369054692 | 5:112,418,665 | T/G | — | uncertain significance |
| rs115979302 | 5:112,419,788 | G/C | — | benign |
| rs2150243862 | 5:112,419,813 | T/A | — | uncertain significance |
| rs146838176 | 5:112,419,832 | C/T | — | uncertain significance |
| rs758016956 | 5:112,420,866 | C/T | — | uncertain significance |
| rs781331890 | 5:112,420,888 | G/A | — | likely benign |
| rs199886106 | 5:112,420,946 | C/T | — | uncertain significance |
| rs756023528 | 5:112,420,956 | T/G | — | uncertain significance |
| rs12513669 | 5:112,427,223 | A/G | — | — |
| rs13436688 | 5:112,430,210 | C/T | intron variant | — |
| rs1756425269 | 5:112,437,449 | C/T | — | uncertain significance |
| rs779948669 | 5:112,437,489 | T/C | — | uncertain significance |
| rs746683962 | 5:112,437,611 | C/T | — | uncertain significance |
| rs6594681 | 5:112,439,941 | T/G | missense variant | — |
| rs1374279707 | 5:112,439,951 | C/T | — | uncertain significance |
| rs138865235 | 5:112,439,957 | C/T | — | uncertain significance |
| rs377175107 | 5:112,439,986 | C/A | — | uncertain significance |
| rs4078252 | 5:112,455,467 | C/T | regulatory region variant | — |
| rs113387336 | 5:112,458,384 | T/C | — | uncertain significance |
| rs1181434315 | 5:112,458,412 | T/A | — | uncertain significance |
| rs1178596450 | 5:112,458,431 | G/T | — | uncertain significance |
| rs148748929 | 5:112,458,479 | C/T | — | likely benign |
| rs146810871 | 5:112,458,489 | G/A | — | uncertain significance |
| rs199896071 | 5:112,458,514 | A/T | — | uncertain significance |
| rs200054847 | 5:112,458,515 | T/A | — | uncertain significance |
| rs750526696 | 5:112,478,956 | C/T | — | likely benign |
| rs1158065160 | 5:112,478,958 | C/T | — | uncertain significance |
| rs372448544 | 5:112,478,985 | T/C | — | uncertain significance |
| rs141072629 | 5:112,478,990 | T/C | — | uncertain significance |
| rs760873189 | 5:112,478,999 | C/T | — | uncertain significance |
| rs377332690 | 5:112,479,008 | G/A | — | uncertain significance |
| rs149028723 | 5:112,479,011 | C/T | — | uncertain significance |
| rs539952782 | 5:112,479,028 | A/C | — | uncertain significance |
| rs145896080 | 5:112,479,043 | G/T | — | uncertain significance |
| rs138719533 | 5:112,479,049 | C/G | — | uncertain significance |
| rs762698185 | 5:112,479,050 | T/C | — | uncertain significance |
| rs202120785 | 5:112,479,054 | C/T | — | uncertain significance |
| rs766574371 | 5:112,479,057 | A/G | — | uncertain significance |
| rs1353702331 | 5:112,487,101 | C/G | — | uncertain significance |
| rs7737490 | 5:112,496,089 | T/C | — | — |
| rs12656003 | 5:112,534,888 | A/T | — | — |
| rs10519339 | 5:112,546,477 | G/A | intron variant | — |
| rs76206262 | 5:112,556,503 | C/A | — | — |
| rs17323670 | 5:112,580,290 | T/C | intron variant | — |
| rs77843857 | 5:112,615,417 | A/G | intron variant | — |
| rs11241200 | 5:112,675,099 | T/A | — | — |
| rs141953753 | 5:112,676,220 | T/C | — | uncertain significance |
Showing 100 of 122 variants. Use the SNP search for the full list.
Gene information from NCBI Gene. Variant classifications from ClinVar.