TMEM245
transmembrane protein 245
Summary
Predicted to be located in membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants50 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs371529090 | 9:111,782,760 | G/C | — | uncertain significance |
| rs145921138 | 9:111,789,006 | T/A | intron variant | — |
| rs368980340 | 9:111,795,588 | G/A | — | uncertain significance |
| rs768956169 | 9:111,795,656 | G/C | — | uncertain significance |
| rs200726668 | 9:111,795,699 | T/C | — | uncertain significance |
| rs753399513 | 9:111,798,559 | C/T | — | uncertain significance |
| rs643410 | 9:111,799,563 | A/G | — | — |
| rs75472294 | 9:111,804,239 | G/A | downstream gene variant | — |
| rs11792861 | 9:111,809,295 | A/C | upstream gene variant | — |
| rs1480492803 | 9:111,812,638 | A/G | — | uncertain significance |
| rs201913195 | 9:111,812,925 | C/G | — | likely benign |
| rs1003346 | 9:111,815,340 | C/A | intron variant | — |
| rs1321045416 | 9:111,819,549 | C/G | — | uncertain significance |
| rs753768436 | 9:111,819,553 | C/T | — | uncertain significance |
| rs201566707 | 9:111,819,564 | C/A | — | uncertain significance |
| rs369367599 | 9:111,819,584 | T/C | — | uncertain significance |
| rs7866966 | 9:111,820,262 | C/T | intron variant | — |
| rs776016549 | 9:111,822,708 | C/A | — | uncertain significance |
| rs1303849672 | 9:111,835,663 | G/A | — | uncertain significance |
| rs760394045 | 9:111,835,697 | T/C | — | uncertain significance |
| rs1358110383 | 9:111,849,498 | C/A | — | uncertain significance |
| rs755180133 | 9:111,849,535 | C/T | — | uncertain significance |
| rs369321391 | 9:111,849,545 | T/C | — | likely benign |
| rs75948484 | 9:111,849,575 | G/A | — | benign |
| rs776757646 | 9:111,849,583 | A/G | — | uncertain significance |
| rs894507082 | 9:111,849,610 | T/C | — | uncertain significance |
| rs370760612 | 9:111,853,210 | G/C | — | uncertain significance |
| rs747782537 | 9:111,853,336 | C/A | — | uncertain significance |
| rs199515741 | 9:111,853,375 | G/C | — | uncertain significance |
| rs761907832 | 9:111,853,390 | G/A | — | uncertain significance |
| rs533132044 | 9:111,853,424 | T/C | — | uncertain significance |
| rs523340 | 9:111,854,246 | G/A | intron variant | — |
| rs776056667 | 9:111,855,806 | T/C | — | uncertain significance |
| rs1830063672 | 9:111,855,839 | C/T | — | uncertain significance |
| rs201071408 | 9:111,870,801 | T/C | — | uncertain significance |
| rs2538469687 | 9:111,881,677 | C/A | — | uncertain significance |
| rs1020425903 | 9:111,881,749 | G/A | — | uncertain significance |
| rs1240441995 | 9:111,881,781 | A/T | — | uncertain significance |
| rs1830841832 | 9:111,881,844 | G/T | — | uncertain significance |
| rs982587248 | 9:111,881,847 | T/C | — | uncertain significance |
| rs145560454 | 9:111,881,973 | T/C | — | likely benign |
| rs2538474343 | 9:111,882,013 | G/C | — | uncertain significance |
| rs1009004783 | 9:111,882,072 | G/A | — | uncertain significance |
| rs1019471090 | 9:111,882,105 | C/T | — | uncertain significance |
| rs2538475504 | 9:111,882,124 | G/A | — | uncertain significance |
| rs763557448 | 9:111,882,149 | G/C | — | uncertain significance |
| rs574526692 | 9:111,882,168 | T/G | — | uncertain significance |
| rs542799910 | 9:111,882,169 | C/T | — | uncertain significance |
| rs528527374 | 9:111,882,172 | T/C | — | uncertain significance |
| rs763805526 | 9:111,882,186 | T/C | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.