MAN1C1
mannosidase alpha class 1C member 1
Summary
Predicted to enable mannosyl-oligosaccharide 1,2-alpha-mannosidase activity. Predicted to be involved in ERAD pathway. Located in extracellular exosome. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants42 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs781600564 | 1:25,944,328 | C/T | — | uncertain significance |
| rs2524352258 | 1:25,944,356 | T/C | — | uncertain significance |
| rs767840940 | 1:25,944,367 | C/T | — | uncertain significance |
| rs2982320 | 1:25,944,454 | C/G | — | benign |
| rs527879949 | 1:25,944,457 | C/T | — | uncertain significance |
| rs745975658 | 1:25,944,542 | C/T | — | uncertain significance |
| rs564755166 | 1:25,944,595 | C/T | — | uncertain significance |
| rs1380491267 | 1:25,944,617 | G/C | — | uncertain significance |
| rs1359609068 | 1:25,944,643 | G/A | — | uncertain significance |
| rs2524354342 | 1:25,944,646 | G/A | — | uncertain significance |
| rs746317826 | 1:25,944,710 | T/C | — | uncertain significance |
| rs2045144462 | 1:25,944,763 | A/G | — | uncertain significance |
| rs1449501588 | 1:25,944,805 | G/A | — | uncertain significance |
| rs12728258 | 1:25,971,646 | T/C | coding sequence variant | — |
| rs181721303 | 1:25,977,444 | T/C | intron variant | — |
| rs12032634 | 1:26,007,568 | T/G | — | — |
| rs375175751 | 1:26,012,961 | C/T | — | uncertain significance |
| rs147313933 | 1:26,012,988 | C/T | — | uncertain significance |
| rs116009723 | 1:26,075,748 | C/T | — | benign |
| rs146745645 | 1:26,075,769 | G/A | — | likely benign |
| rs377564466 | 1:26,079,978 | T/C | — | uncertain significance |
| rs574993256 | 1:26,079,982 | G/A | — | uncertain significance |
| rs757838115 | 1:26,080,053 | G/A | — | uncertain significance |
| rs2524782350 | 1:26,080,054 | T/C | — | uncertain significance |
| rs201284037 | 1:26,085,106 | C/T | — | uncertain significance |
| rs544511408 | 1:26,090,437 | G/A | — | uncertain significance |
| rs2524862479 | 1:26,098,217 | G/A | — | uncertain significance |
| rs573023765 | 1:26,098,251 | C/T | — | likely benign |
| rs746164670 | 1:26,104,755 | C/T | — | uncertain significance |
| rs146718720 | 1:26,104,810 | G/A | — | uncertain significance |
| rs375066144 | 1:26,107,469 | G/A | — | uncertain significance |
| rs1228948770 | 1:26,107,477 | G/A | — | likely benign |
| rs1202008079 | 1:26,107,574 | T/C | — | uncertain significance |
| rs760943548 | 1:26,109,094 | C/T | — | uncertain significance |
| rs150201998 | 1:26,109,126 | C/T | — | likely benign |
| rs1424350166 | 1:26,109,151 | G/A | — | uncertain significance |
| rs139260749 | 1:26,109,180 | G/A | — | likely benign |
| rs371173401 | 1:26,109,200 | T/C | — | likely benign |
| rs187331964 | 1:26,110,150 | A/G | — | likely benign |
| rs79893268 | 1:26,110,151 | C/T | — | benign |
| rs1194004257 | 1:26,110,161 | T/C | — | uncertain significance |
| rs79507311 | 1:26,110,236 | G/A | missense variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.