CARMIL1
capping protein regulator and myosin 1 linker 1
Summary
Involved in several processes, including actin filament network formation; plasma membrane bounded cell projection organization; and positive regulation of cellular component organization. Located in several cellular components, including lamellipodium; macropinosome; and nuclear speck. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants54 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1412088464 | 6:25,280,033 | G/C | — | uncertain significance |
| rs144350646 | 6:25,283,177 | A/G | downstream gene variant | — |
| rs2064206 | 6:25,291,070 | G/A | upstream gene variant | — |
| rs183360145 | 6:25,297,121 | T/C | regulatory region variant | — |
| rs4712905 | 6:25,306,732 | C/G | — | — |
| rs190770638 | 6:25,314,816 | A/G | intron variant | — |
| rs71555190 | 6:25,333,665 | G/A | intron variant | — |
| rs12196438 | 6:25,334,241 | C/T | intron variant | — |
| rs2744228 | 6:25,341,405 | T/G | regulatory region variant | — |
| rs2690093 | 6:25,344,987 | G/A | intron variant | — |
| rs79693813 | 6:25,345,251 | G/A | — | — |
| rs2744239 | 6:25,356,350 | A/G | intron variant | — |
| rs116418977 | 6:25,365,888 | C/T | intron variant | — |
| rs77925174 | 6:25,368,194 | G/T | intron variant | — |
| rs9348676 | 6:25,398,426 | T/A | — | — |
| rs13216709 | 6:25,403,327 | T/A | — | — |
| rs79774308 | 6:25,411,022 | A/G | downstream gene variant | — |
| rs9467508 | 6:25,421,747 | A/T | — | — |
| rs58657257 | 6:25,426,061 | T/C | intron variant | — |
| rs9358856 | 6:25,426,768 | G/A | missense variant | — |
| rs535816044 | 6:25,428,517 | A/G | — | — |
| rs77371797 | 6:25,455,534 | A/C | — | — |
| rs301400 | 6:25,464,108 | T/C | intron variant | — |
| rs301399 | 6:25,464,199 | C/T | intron variant | — |
| rs149124714 | 6:25,469,271 | G/A | intron variant | — |
| rs41271813 | 6:25,472,490 | A/G | intron variant | — |
| rs2274089 | 6:25,488,583 | C/T | intron variant | — |
| rs16890655 | 6:25,488,925 | A/G | intron variant | — |
| rs562682035 | 6:25,490,974 | T/A | — | — |
| rs370215465 | 6:25,495,362 | C/A | — | uncertain significance |
| rs2769701 | 6:25,507,624 | A/G | intron variant | — |
| rs212938 | 6:25,522,443 | A/G | intron variant | — |
| rs149359690 | 6:25,526,319 | C/T | intron variant | — |
| rs6913974 | 6:25,528,550 | G/A | intron variant | — |
| rs214056 | 6:25,530,084 | G/C | intron variant | — |
| rs214058 | 6:25,531,368 | G/T | — | — |
| rs12526480 | 6:25,533,534 | T/G | intron variant | — |
| rs77244967 | 6:25,536,591 | A/C | intron variant | — |
| rs214059 | 6:25,536,937 | C/T | intron variant | — |
| rs214060 | 6:25,537,194 | C/G | — | — |
| rs201096469 | 6:25,540,215 | C/T | — | uncertain significance |
| rs969297 | 6:25,543,639 | G/A | intron variant | — |
| rs79276065 | 6:25,547,484 | G/A | intron variant | — |
| rs441460 | 6:25,548,288 | G/T | — | — |
| rs11968608 | 6:25,553,812 | T/G | intron variant | — |
| rs72839085 | 6:25,575,053 | A/C | intron variant | — |
| rs926326 | 6:25,575,402 | A/G | intron variant | — |
| rs373726074 | 6:25,581,512 | A/G | — | uncertain significance |
| rs28393611 | 6:25,586,946 | C/G | — | — |
| rs7766874 | 6:25,589,165 | A/G | intron variant | — |
| rs182293263 | 6:25,600,559 | G/A | — | uncertain significance |
| rs527331116 | 6:25,600,667 | G/A | — | uncertain significance |
| rs2536334365 | 6:25,600,750 | G/A | — | uncertain significance |
| rs742132 | 6:25,607,571 | A/G | intron variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.