TMEM132A
transmembrane protein 132A
Summary
This gene encodes a protein that is highly similar to the rat Grp78-binding protein (GBP). Alternatively spliced transcript variants encoding different isoforms have been described. [provided by RefSeq, Jul 2008]
Known Variants78 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs745831135 | 11:60,692,127 | C/G | — | uncertain significance |
| rs2539102649 | 11:60,692,166 | C/G | — | uncertain significance |
| rs773906622 | 11:60,694,858 | C/T | — | uncertain significance |
| rs144704995 | 11:60,695,126 | G/A | — | uncertain significance |
| rs758917002 | 11:60,695,146 | C/T | — | uncertain significance |
| rs1856377492 | 11:60,695,161 | G/C | — | uncertain significance |
| rs114893240 | 11:60,695,163 | C/T | — | benign |
| rs373031720 | 11:60,695,167 | C/T | — | uncertain significance |
| rs1320764931 | 11:60,695,203 | G/A | — | uncertain significance |
| rs369462368 | 11:60,695,309 | C/T | — | uncertain significance |
| rs777651889 | 11:60,695,318 | C/G | — | uncertain significance |
| rs144441365 | 11:60,695,324 | G/A | — | uncertain significance |
| rs180968764 | 11:60,695,429 | C/T | downstream gene variant | — |
| rs768321505 | 11:60,696,113 | G/A | — | uncertain significance |
| rs771413372 | 11:60,696,119 | G/A | — | uncertain significance |
| rs140412965 | 11:60,696,171 | G/T | — | uncertain significance |
| rs370425430 | 11:60,696,213 | C/G | — | uncertain significance |
| rs77946216 | 11:60,696,284 | C/T | — | uncertain significance |
| rs539239034 | 11:60,696,359 | G/T | — | uncertain significance |
| rs372811050 | 11:60,696,368 | G/A | — | uncertain significance |
| rs145130532 | 11:60,696,392 | C/A | — | uncertain significance |
| rs773354003 | 11:60,696,431 | C/T | — | uncertain significance |
| rs79424635 | 11:60,696,448 | C/T | upstream gene variant | — |
| rs1331660491 | 11:60,698,065 | A/G | — | uncertain significance |
| rs150894243 | 11:60,698,104 | G/A | — | uncertain significance |
| rs2074414 | 11:60,698,712 | A/G | intron variant | — |
| rs11230521 | 11:60,698,732 | G/A | intron variant | — |
| rs138156166 | 11:60,699,165 | C/G | — | uncertain significance |
| rs899958405 | 11:60,699,219 | G/T | — | uncertain significance |
| rs147239477 | 11:60,699,225 | G/A | — | uncertain significance |
| rs748299271 | 11:60,699,229 | C/G | — | uncertain significance |
| rs773336173 | 11:60,699,237 | C/T | — | uncertain significance |
| rs2539113508 | 11:60,699,296 | A/C | — | uncertain significance |
| rs566097839 | 11:60,699,513 | C/T | — | uncertain significance |
| rs573630966 | 11:60,699,567 | G/A | — | uncertain significance |
| rs1300777048 | 11:60,701,066 | C/T | — | uncertain significance |
| rs369347951 | 11:60,701,067 | C/T | — | likely benign |
| rs772486219 | 11:60,701,068 | C/T | — | uncertain significance |
| rs769961709 | 11:60,701,104 | C/T | — | uncertain significance |
| rs1323267189 | 11:60,701,107 | G/T | — | uncertain significance |
| rs1315116635 | 11:60,701,149 | C/T | — | uncertain significance |
| rs2539117952 | 11:60,701,968 | A/G | — | uncertain significance |
| rs933605439 | 11:60,702,006 | G/A | — | uncertain significance |
| rs2539118192 | 11:60,702,046 | G/A | — | uncertain significance |
| rs2539118203 | 11:60,702,049 | T/G | — | uncertain significance |
| rs966375456 | 11:60,702,055 | C/T | — | likely benign |
| rs776316834 | 11:60,702,058 | C/G | — | uncertain significance |
| rs764720498 | 11:60,702,064 | C/T | — | uncertain significance |
| rs772710922 | 11:60,702,077 | G/A | — | likely benign |
| rs762480999 | 11:60,702,159 | G/A | — | uncertain significance |
| rs199985864 | 11:60,702,163 | T/C | missense variant | — |
| rs150311425 | 11:60,702,192 | G/A | — | uncertain significance |
| rs756914665 | 11:60,702,727 | C/G | — | uncertain significance |
| rs371074568 | 11:60,702,764 | C/T | — | uncertain significance |
| rs1856587014 | 11:60,703,448 | T/A | — | uncertain significance |
| rs1039552485 | 11:60,703,478 | T/C | — | uncertain significance |
| rs376877652 | 11:60,703,480 | G/A | — | uncertain significance |
| rs578062643 | 11:60,703,492 | A/G | — | uncertain significance |
| rs111231672 | 11:60,703,542 | C/A | — | benign |
| rs550430630 | 11:60,703,562 | G/A | — | uncertain significance |
| rs779758743 | 11:60,703,606 | C/T | — | uncertain significance |
| rs1379344217 | 11:60,703,639 | T/A | — | uncertain significance |
| rs201227499 | 11:60,703,711 | G/A | — | uncertain significance |
| rs2539122126 | 11:60,703,715 | G/A | — | likely benign |
| rs1490307412 | 11:60,703,808 | A/T | — | uncertain significance |
| rs142571833 | 11:60,703,876 | T/C | — | uncertain significance |
| rs551776907 | 11:60,703,975 | C/T | — | uncertain significance |
| rs372456749 | 11:60,704,054 | C/T | — | likely benign |
| rs762597307 | 11:60,704,122 | G/C | — | uncertain significance |
| rs756642343 | 11:60,704,132 | G/C | — | uncertain significance |
| rs559986342 | 11:60,704,138 | C/T | — | uncertain significance |
| rs200710128 | 11:60,704,156 | C/A | — | uncertain significance |
| rs746092283 | 11:60,704,162 | C/G | — | uncertain significance |
| rs146870859 | 11:60,704,183 | G/A | — | uncertain significance |
| rs149340923 | 11:60,704,236 | C/T | — | uncertain significance |
| rs755179853 | 11:60,704,239 | G/A | — | uncertain significance |
| rs368115669 | 11:60,704,299 | C/T | — | uncertain significance |
| rs376130640 | 11:60,704,366 | G/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.