TMCC2
transmembrane and coiled-coil domain family 2
Summary
Involved in amyloid precursor protein metabolic process. Located in endoplasmic reticulum. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants60 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1337805052 | 1:205,197,757 | A/G | — | uncertain significance |
| rs201910975 | 1:205,197,762 | G/A | — | uncertain significance |
| rs1659662740 | 1:205,197,796 | C/A | — | uncertain significance |
| rs144151238 | 1:205,197,807 | A/G | — | likely benign |
| rs556554804 | 1:205,197,840 | G/A | — | uncertain significance |
| rs10793727 | 1:205,199,200 | A/T | — | — |
| rs12126439 | 1:205,200,720 | C/T | downstream gene variant | — |
| rs113043890 | 1:205,203,353 | C/T | intron variant | — |
| rs4951179 | 1:205,205,072 | G/T | — | — |
| rs11240396 | 1:205,205,081 | T/G | — | — |
| rs751531683 | 1:205,210,646 | T/C | — | uncertain significance |
| rs1558645095 | 1:205,210,654 | G/A | — | uncertain significance |
| rs552285360 | 1:205,210,703 | G/A | — | uncertain significance |
| rs138497244 | 1:205,210,709 | G/A | — | uncertain significance |
| rs2464505110 | 1:205,210,766 | T/C | — | uncertain significance |
| rs77588763 | 1:205,210,827 | C/A | — | uncertain significance |
| rs1346681758 | 1:205,210,906 | A/G | — | uncertain significance |
| rs1261820035 | 1:205,210,913 | G/A | — | uncertain significance |
| rs1660277461 | 1:205,210,916 | G/A | — | uncertain significance |
| rs1305201676 | 1:205,210,943 | G/T | — | uncertain significance |
| rs534966945 | 1:205,210,945 | G/A | — | uncertain significance |
| rs201528355 | 1:205,210,952 | G/A | — | uncertain significance |
| rs200029580 | 1:205,211,000 | G/A | — | uncertain significance |
| rs375718104 | 1:205,211,021 | G/A | — | uncertain significance |
| rs149416299 | 1:205,211,053 | A/G | — | benign |
| rs775807545 | 1:205,211,096 | C/T | — | uncertain significance |
| rs753557919 | 1:205,211,122 | G/A | — | uncertain significance |
| rs146720283 | 1:205,211,131 | G/A | — | uncertain significance |
| rs369237599 | 1:205,211,164 | G/A | — | uncertain significance |
| rs11240397 | 1:205,211,182 | G/A | — | benign |
| rs185025114 | 1:205,213,103 | G/A | intron variant | — |
| rs7368327 | 1:205,214,792 | C/T | intron variant | — |
| rs1172152 | 1:205,220,718 | T/A | intron variant | — |
| rs76133172 | 1:205,220,994 | A/G | intron variant | — |
| rs570903956 | 1:205,227,294 | C/T | — | — |
| rs11588057 | 1:205,234,575 | C/T | intron variant | — |
| rs1668873 | 1:205,235,990 | G/A | intron variant | — |
| rs542661060 | 1:205,236,935 | T/C | — | — |
| rs1668871 | 1:205,237,137 | T/G | — | — |
| rs370713286 | 1:205,238,130 | C/G | — | uncertain significance |
| rs201477018 | 1:205,238,135 | G/T | — | uncertain significance |
| rs137961859 | 1:205,238,158 | C/T | — | benign |
| rs372274523 | 1:205,238,169 | C/T | — | uncertain significance |
| rs1040976052 | 1:205,238,258 | C/T | — | uncertain significance |
| rs750784398 | 1:205,238,270 | G/T | — | uncertain significance |
| rs1432444465 | 1:205,238,324 | A/G | — | uncertain significance |
| rs1353178274 | 1:205,238,357 | T/C | — | uncertain significance |
| rs774336922 | 1:205,238,456 | G/A | — | uncertain significance |
| rs1167646058 | 1:205,238,508 | C/T | — | uncertain significance |
| rs201081913 | 1:205,238,627 | C/T | — | uncertain significance |
| rs7538074 | 1:205,238,716 | C/T | — | benign |
| rs1768584 | 1:205,240,145 | A/G | regulatory region variant | — |
| rs9659978 | 1:205,240,913 | A/G | intron variant | — |
| rs150581410 | 1:205,240,947 | G/A | — | uncertain significance |
| rs140687186 | 1:205,241,056 | A/G | — | uncertain significance |
| rs761361801 | 1:205,241,103 | G/A | — | uncertain significance |
| rs756092641 | 1:205,241,128 | C/T | — | uncertain significance |
| rs2464633189 | 1:205,241,137 | T/C | — | uncertain significance |
| rs139249543 | 1:205,242,769 | A/T | regulatory region variant | — |
| rs1172132 | 1:205,242,901 | A/G | regulatory region variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.