TMEM132C
transmembrane protein 132C
Summary
Predicted to be located in membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants109 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs570055209 | 12:128,751,961 | G/A | — | uncertain significance |
| rs7979166 | 12:128,768,520 | C/T | intron variant | — |
| rs28654182 | 12:128,769,038 | A/G | intron variant | — |
| rs11059635 | 12:128,782,022 | C/G | — | — |
| rs952093 | 12:128,844,571 | T/A | — | — |
| rs768707329 | 12:128,899,291 | G/A | — | uncertain significance |
| rs1488172613 | 12:128,899,308 | A/G | — | uncertain significance |
| rs1457918234 | 12:128,899,319 | C/T | — | uncertain significance |
| rs765415062 | 12:128,899,330 | C/A | — | uncertain significance |
| rs371034880 | 12:128,899,368 | G/T | — | uncertain significance |
| rs373303227 | 12:128,899,408 | C/T | — | uncertain significance |
| rs370341069 | 12:128,899,478 | A/G | — | uncertain significance |
| rs370488183 | 12:128,899,529 | T/G | — | uncertain significance |
| rs375036389 | 12:128,899,533 | G/T | — | uncertain significance |
| rs757809537 | 12:128,899,559 | A/G | — | likely benign |
| rs373791897 | 12:128,899,601 | G/A | — | uncertain significance |
| rs769440363 | 12:128,899,621 | C/T | — | uncertain significance |
| rs372788590 | 12:128,899,648 | A/G | — | likely benign |
| rs557263376 | 12:128,899,747 | C/T | — | uncertain significance |
| rs760872130 | 12:128,899,817 | C/T | — | uncertain significance |
| rs573315759 | 12:128,899,827 | C/T | — | likely benign |
| rs767224820 | 12:128,899,845 | G/C | — | uncertain significance |
| rs770103092 | 12:128,899,852 | C/G | — | uncertain significance |
| rs200339631 | 12:128,899,853 | C/T | — | uncertain significance |
| rs12307622 | 12:128,899,885 | G/A | — | benign |
| rs1009922915 | 12:128,899,942 | G/A | — | uncertain significance |
| rs374760970 | 12:128,899,991 | A/G | — | uncertain significance |
| rs190556433 | 12:128,899,998 | C/T | — | likely benign |
| rs200249610 | 12:128,900,032 | G/A | — | uncertain significance |
| rs911167411 | 12:128,900,050 | C/T | — | uncertain significance |
| rs781305645 | 12:128,900,089 | C/T | — | uncertain significance |
| rs1215883871 | 12:128,900,150 | A/G | — | uncertain significance |
| rs4882760 | 12:128,913,894 | A/C | — | — |
| rs1075399 | 12:128,947,559 | T/G | — | — |
| rs1274387343 | 12:129,028,518 | G/T | — | uncertain significance |
| rs760351876 | 12:129,028,526 | C/G | — | uncertain significance |
| rs1164077612 | 12:129,028,546 | G/A | — | uncertain significance |
| rs1353532995 | 12:129,028,554 | C/T | — | uncertain significance |
| rs373744713 | 12:129,028,566 | G/A | — | uncertain significance |
| rs372279119 | 12:129,028,587 | G/A | — | uncertain significance |
| rs781327334 | 12:129,028,590 | G/A | — | uncertain significance |
| rs541595581 | 12:129,028,614 | G/A | — | uncertain significance |
| rs561801857 | 12:129,028,619 | C/T | — | likely benign |
| rs542492963 | 12:129,068,436 | C/T | — | — |
| rs144288546 | 12:129,069,682 | G/A | intron variant | — |
| rs141689732 | 12:129,094,290 | G/A | intron variant | — |
| rs7296262 | 12:129,095,072 | T/G | — | — |
| rs1386304616 | 12:129,100,722 | G/C | — | uncertain significance |
| rs1565992551 | 12:129,100,741 | T/C | — | uncertain significance |
| rs768129682 | 12:129,100,801 | G/A | — | uncertain significance |
| rs189652448 | 12:129,100,822 | C/T | — | uncertain significance |
| rs779054139 | 12:129,153,965 | A/G | — | uncertain significance |
| rs542076193 | 12:129,154,070 | G/A | — | uncertain significance |
| rs140584108 | 12:129,178,435 | C/T | — | likely benign |
| rs186918525 | 12:129,178,450 | C/T | — | uncertain significance |
| rs776505881 | 12:129,178,485 | G/A | — | uncertain significance |
| rs775344947 | 12:129,178,498 | G/A | — | uncertain significance |
| rs2541082207 | 12:129,180,424 | G/A | — | uncertain significance |
| rs948864796 | 12:129,180,460 | G/A | — | uncertain significance |
| rs113503516 | 12:129,180,487 | G/A | — | uncertain significance |
| rs553310471 | 12:129,180,490 | G/C | — | uncertain significance |
| rs945612301 | 12:129,180,506 | C/T | — | likely benign |
| rs575727630 | 12:129,180,608 | G/A | — | uncertain significance |
| rs1229358538 | 12:129,181,817 | G/A | — | uncertain significance |
| rs1249494714 | 12:129,181,849 | G/T | — | uncertain significance |
| rs1370459443 | 12:129,181,890 | C/A | — | uncertain significance |
| rs1273953125 | 12:129,181,911 | C/T | — | uncertain significance |
| rs201956806 | 12:129,181,946 | C/T | — | uncertain significance |
| rs10773568 | 12:129,186,190 | G/A | intron variant | — |
| rs1004081678 | 12:129,189,675 | C/G | — | uncertain significance |
| rs777057937 | 12:129,189,764 | C/T | — | uncertain significance |
| rs892404178 | 12:129,189,776 | T/C | — | uncertain significance |
| rs576055853 | 12:129,189,782 | G/A | — | uncertain significance |
| rs776145107 | 12:129,189,821 | C/G | — | uncertain significance |
| rs1367653480 | 12:129,189,861 | A/G | — | uncertain significance |
| rs545600869 | 12:129,189,887 | G/A | — | likely benign |
| rs1295618091 | 12:129,189,938 | G/A | — | uncertain significance |
| rs919803681 | 12:129,189,986 | C/T | — | uncertain significance |
| rs780371502 | 12:129,190,049 | G/A | — | uncertain significance |
| rs772510769 | 12:129,190,055 | C/T | — | uncertain significance |
| rs1287005938 | 12:129,190,061 | G/C | — | uncertain significance |
| rs866216098 | 12:129,190,182 | T/C | — | uncertain significance |
| rs529595183 | 12:129,190,185 | A/T | — | uncertain significance |
| rs768535689 | 12:129,190,226 | G/A | — | uncertain significance |
| rs1003095535 | 12:129,190,249 | C/A | — | uncertain significance |
| rs948229795 | 12:129,190,263 | C/T | — | uncertain significance |
| rs560254297 | 12:129,190,421 | G/A | — | uncertain significance |
| rs1347145172 | 12:129,190,426 | G/T | — | uncertain significance |
| rs1181592725 | 12:129,190,473 | C/T | — | uncertain significance |
| rs979600538 | 12:129,190,476 | C/T | — | uncertain significance |
| rs753269750 | 12:129,190,512 | G/A | — | uncertain significance |
| rs528438138 | 12:129,190,514 | G/A | — | uncertain significance |
| rs1954836720 | 12:129,190,515 | G/T | — | uncertain significance |
| rs775094218 | 12:129,190,523 | G/A | — | uncertain significance |
| rs779428852 | 12:129,190,529 | G/A | — | uncertain significance |
| rs2541089716 | 12:129,190,619 | G/A | — | uncertain significance |
| rs752030046 | 12:129,190,639 | C/A | — | likely benign |
| rs944283043 | 12:129,190,650 | C/T | — | uncertain significance |
| rs2541089767 | 12:129,190,659 | C/G | — | uncertain significance |
| rs1197227746 | 12:129,190,694 | A/G | — | uncertain significance |
Showing 100 of 109 variants. Use the SNP search for the full list.
Gene information from NCBI Gene. Variant classifications from ClinVar.