CD109
CD109 molecule
Summary
This gene encodes a glycosyl phosphatidylinositol (GPI)-linked glycoprotein that localizes to the surface of platelets, activated T-cells, and endothelial cells. The protein binds to and negatively regulates signalling by transforming growth factor beta (TGF-beta). Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Apr 2014]
Known Variants134 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs565430659 | 6:74,395,900 | G/C | — | — |
| rs79717953 | 6:74,404,771 | C/T | coding sequence variant | — |
| rs920184106 | 6:74,405,946 | G/T | — | uncertain significance |
| rs941441710 | 6:74,406,008 | C/T | — | uncertain significance |
| rs202157387 | 6:74,407,127 | C/T | — | uncertain significance |
| rs2533612809 | 6:74,407,148 | G/A | — | uncertain significance |
| rs767347688 | 6:74,407,227 | C/T | — | uncertain significance |
| rs141000744 | 6:74,407,257 | C/G | — | uncertain significance |
| rs143135810 | 6:74,417,888 | C/G | intron variant | — |
| rs9446991 | 6:74,418,273 | T/G | intron variant | — |
| rs549784614 | 6:74,421,248 | G/A | — | — |
| rs9442950 | 6:74,423,728 | C/T | regulatory region variant | — |
| rs181389471 | 6:74,431,162 | G/T | — | — |
| rs147342140 | 6:74,440,124 | G/A | — | uncertain significance |
| rs1421308224 | 6:74,440,135 | A/T | — | uncertain significance |
| rs2533734326 | 6:74,440,286 | A/T | — | uncertain significance |
| rs746314222 | 6:74,446,196 | A/G | — | uncertain significance |
| rs148575660 | 6:74,446,214 | G/A | — | benign |
| rs140225211 | 6:74,450,742 | G/A | intron variant | — |
| rs192957332 | 6:74,454,426 | A/G | intron variant | — |
| rs114709397 | 6:74,456,035 | C/T | intron variant | — |
| rs146504307 | 6:74,458,240 | T/C | intron variant | — |
| rs9447004 | 6:74,458,737 | A/G | intron variant | — |
| rs370813601 | 6:74,466,403 | A/G | — | uncertain significance |
| rs117457886 | 6:74,466,613 | A/G | intron variant | — |
| rs41265525 | 6:74,466,676 | T/G | intron variant | — |
| rs762625249 | 6:74,468,714 | A/G | — | uncertain significance |
| rs2533853064 | 6:74,468,718 | A/G | — | uncertain significance |
| rs199660260 | 6:74,468,745 | C/T | — | uncertain significance |
| rs374417084 | 6:74,472,465 | T/C | — | uncertain significance |
| rs1018104990 | 6:74,472,503 | A/G | — | uncertain significance |
| rs765802724 | 6:74,472,561 | C/G | — | uncertain significance |
| rs912040605 | 6:74,473,349 | A/G | — | uncertain significance |
| rs188913865 | 6:74,474,807 | T/C | intron variant | — |
| rs7741152 | 6:74,475,675 | G/A | — | benign |
| rs185952786 | 6:74,475,686 | A/T | — | uncertain significance |
| rs146419763 | 6:74,475,690 | T/C | — | likely benign |
| rs113690012 | 6:74,475,791 | C/G | — | likely benign |
| rs760270113 | 6:74,475,793 | G/C | — | uncertain significance |
| rs377190899 | 6:74,475,812 | C/T | — | uncertain significance |
| rs758964670 | 6:74,475,818 | A/C | — | uncertain significance |
| rs1381925785 | 6:74,476,486 | A/G | — | uncertain significance |
| rs1424001051 | 6:74,476,490 | C/G | — | uncertain significance |
| rs770774095 | 6:74,476,667 | C/T | — | likely benign |
| rs201376556 | 6:74,476,678 | C/T | — | uncertain significance |
| rs779693948 | 6:74,476,731 | A/G | — | uncertain significance |
| rs2533901570 | 6:74,477,808 | G/A | — | uncertain significance |
| rs762332426 | 6:74,477,895 | G/C | — | uncertain significance |
| rs190600286 | 6:74,479,200 | G/A | intron variant | — |
| rs62438668 | 6:74,480,354 | C/T | intron variant | — |
| rs2533914529 | 6:74,481,164 | T/G | — | uncertain significance |
| rs41266745 | 6:74,481,186 | C/T | missense variant | Likely benign |
| rs367954593 | 6:74,481,221 | C/G | — | uncertain significance |
| rs140153127 | 6:74,481,225 | C/T | — | uncertain significance |
| rs200189270 | 6:74,481,233 | A/G | — | uncertain significance |
| rs4263551 | 6:74,486,371 | T/A | — | — |
| rs9293941 | 6:74,490,344 | A/C | intron variant | — |
| rs939093271 | 6:74,490,992 | T/A | — | uncertain significance |
| rs7742662 | 6:74,491,002 | G/T | — | benign |
| rs2533965714 | 6:74,492,352 | A/G | — | uncertain significance |
| rs1290549152 | 6:74,492,400 | A/G | — | uncertain significance |
| rs376378346 | 6:74,493,471 | C/T | — | uncertain significance |
| rs199617851 | 6:74,493,494 | G/T | — | uncertain significance |
| rs1471687309 | 6:74,493,509 | G/A | — | uncertain significance |
| rs77238980 | 6:74,495,203 | A/G | — | benign |
| rs4706555 | 6:74,496,415 | T/G | intron variant | — |
| rs760476361 | 6:74,497,023 | A/G | — | uncertain significance |
| rs1774735999 | 6:74,497,077 | T/C | — | uncertain significance |
| rs771162654 | 6:74,497,134 | C/T | — | uncertain significance |
| rs1168798738 | 6:74,498,273 | T/C | — | uncertain significance |
| rs764564642 | 6:74,498,290 | C/T | — | uncertain significance |
| rs1313240950 | 6:74,498,324 | T/A | — | uncertain significance |
| rs184996807 | 6:74,502,077 | T/A | intron variant | — |
| rs373931081 | 6:74,502,373 | A/G | — | uncertain significance |
| rs749134372 | 6:74,502,393 | C/G | — | uncertain significance |
| rs1775014477 | 6:74,502,405 | G/A | — | uncertain significance |
| rs1775014643 | 6:74,502,406 | G/T | — | uncertain significance |
| rs2534017217 | 6:74,502,411 | G/A | — | uncertain significance |
| rs773535517 | 6:74,502,462 | C/A | — | uncertain significance |
| rs767770529 | 6:74,502,488 | T/G | — | likely benign |
| rs768313068 | 6:74,502,519 | A/G | — | uncertain significance |
| rs6925924 | 6:74,503,727 | T/C | intron variant | — |
| rs6903575 | 6:74,503,730 | G/A | intron variant | — |
| rs6907989 | 6:74,504,074 | A/T | intron variant | — |
| rs12663978 | 6:74,505,467 | C/A | — | — |
| rs73460398 | 6:74,506,072 | A/G | intron variant | — |
| rs10943130 | 6:74,506,220 | C/T | intron variant | — |
| rs997767 | 6:74,507,011 | A/T | intron variant | — |
| rs76597678 | 6:74,508,197 | C/T | regulatory region variant | — |
| rs4708086 | 6:74,509,052 | A/G | intron variant | — |
| rs555278092 | 6:74,509,221 | C/T | — | — |
| rs57799429 | 6:74,509,578 | G/A | — | — |
| rs1973483 | 6:74,512,687 | C/T | intron variant | — |
| rs41266753 | 6:74,513,719 | C/T | regulatory region variant | — |
| rs574204659 | 6:74,516,603 | C/T | — | likely benign |
| rs143676607 | 6:74,516,649 | A/T | — | conflicting classifications of pathogenicity |
| rs368124542 | 6:74,516,679 | G/A | — | uncertain significance |
| rs1311134093 | 6:74,516,693 | T/A | — | likely benign |
| rs201386395 | 6:74,516,758 | A/T | — | uncertain significance |
| rs749536122 | 6:74,516,788 | A/G | — | uncertain significance |
Showing 100 of 134 variants. Use the SNP search for the full list.
Gene information from NCBI Gene. Variant classifications from ClinVar.