CAMSAP3
calmodulin regulated spectrin associated protein family member 3
Summary
Enables actin filament binding activity and microtubule minus-end binding activity. Involved in several processes, including microtubule cytoskeleton organization; regulation of organelle organization; and zonula adherens maintenance. Located in cytoplasm; microtubule cytoskeleton; and zonula adherens. [provided by Alliance of Genome Resources, Apr 2025]
Known Variants76 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs2146147920 | 19:7,660,896 | A/C | — | uncertain significance |
| rs190020306 | 19:7,665,882 | T/C | intron variant | — |
| rs2512617640 | 19:7,670,121 | C/T | — | uncertain significance |
| rs2512617670 | 19:7,670,129 | C/A | — | uncertain significance |
| rs779334786 | 19:7,670,337 | C/A | — | uncertain significance |
| rs2512620440 | 19:7,671,189 | G/A | — | uncertain significance |
| rs1568441817 | 19:7,671,200 | C/T | — | uncertain significance |
| rs2030220080 | 19:7,671,205 | G/A | — | uncertain significance |
| rs1225722242 | 19:7,671,456 | C/T | — | uncertain significance |
| rs145801118 | 19:7,673,065 | G/A | — | benign |
| rs201177218 | 19:7,673,107 | C/T | — | benign |
| rs201741898 | 19:7,673,122 | C/G | — | uncertain significance |
| rs200223315 | 19:7,675,440 | G/A | — | uncertain significance |
| rs57521028 | 19:7,675,483 | C/T | — | benign |
| rs758790660 | 19:7,675,484 | G/A | — | uncertain significance |
| rs188146738 | 19:7,675,687 | C/T | — | benign |
| rs764938933 | 19:7,675,775 | G/A | — | uncertain significance |
| rs779864414 | 19:7,675,786 | G/T | — | uncertain significance |
| rs377374576 | 19:7,675,799 | A/C | — | uncertain significance |
| rs755140419 | 19:7,676,421 | C/T | — | uncertain significance |
| rs114173574 | 19:7,676,422 | G/A | — | benign |
| rs200525165 | 19:7,676,426 | A/G | — | uncertain significance |
| rs1352706308 | 19:7,676,435 | A/G | — | uncertain significance |
| rs1342514235 | 19:7,676,574 | C/T | — | uncertain significance |
| rs2512629210 | 19:7,676,667 | G/C | — | uncertain significance |
| rs558267944 | 19:7,676,692 | C/A | — | uncertain significance |
| rs769372763 | 19:7,676,704 | C/T | — | uncertain significance |
| rs776610367 | 19:7,676,730 | C/A | — | uncertain significance |
| rs753516379 | 19:7,676,877 | T/C | — | uncertain significance |
| rs200164598 | 19:7,676,959 | C/T | — | uncertain significance |
| rs374239550 | 19:7,677,133 | C/T | — | uncertain significance |
| rs866751877 | 19:7,677,139 | C/T | — | uncertain significance |
| rs199718809 | 19:7,677,151 | C/A | — | uncertain significance |
| rs761356344 | 19:7,677,181 | G/A | — | uncertain significance |
| rs772585276 | 19:7,677,265 | G/A | — | uncertain significance |
| rs138441786 | 19:7,677,354 | G/C | — | likely benign |
| rs763895024 | 19:7,677,417 | A/C | — | uncertain significance |
| rs906506514 | 19:7,677,423 | G/C | — | uncertain significance |
| rs202045562 | 19:7,677,429 | T/A | — | uncertain significance |
| rs200075510 | 19:7,677,430 | T/C | — | uncertain significance |
| rs766535347 | 19:7,677,436 | C/T | — | uncertain significance |
| rs141087775 | 19:7,677,440 | C/G | — | likely benign |
| rs2512631247 | 19:7,677,579 | C/T | — | uncertain significance |
| rs928044292 | 19:7,677,582 | G/A | — | uncertain significance |
| rs572745116 | 19:7,677,628 | C/T | — | uncertain significance |
| rs779477941 | 19:7,677,664 | G/A | — | uncertain significance |
| rs768260718 | 19:7,677,682 | G/A | — | uncertain significance |
| rs1024174137 | 19:7,677,739 | C/T | — | uncertain significance |
| rs2512631785 | 19:7,677,761 | G/T | — | uncertain significance |
| rs2146172347 | 19:7,677,762 | A/T | — | uncertain significance |
| rs750906640 | 19:7,677,820 | C/T | — | uncertain significance |
| rs2030589729 | 19:7,677,892 | C/A | — | uncertain significance |
| rs755873356 | 19:7,677,898 | G/T | — | uncertain significance |
| rs774821513 | 19:7,680,090 | G/C | — | uncertain significance |
| rs61747262 | 19:7,680,190 | G/A | — | benign |
| rs1009890227 | 19:7,680,324 | C/T | — | uncertain significance |
| rs2512636517 | 19:7,680,333 | C/T | — | uncertain significance |
| rs2030731757 | 19:7,680,356 | A/G | — | uncertain significance |
| rs1363371854 | 19:7,680,360 | C/T | — | uncertain significance |
| rs936844181 | 19:7,680,440 | G/A | — | uncertain significance |
| rs1378655270 | 19:7,680,443 | C/T | — | uncertain significance |
| rs2512636876 | 19:7,680,468 | A/G | — | uncertain significance |
| rs888893073 | 19:7,680,594 | G/A | — | uncertain significance |
| rs747562030 | 19:7,681,478 | A/G | — | uncertain significance |
| rs748924614 | 19:7,681,486 | G/A | — | uncertain significance |
| rs201293526 | 19:7,682,223 | C/T | — | uncertain significance |
| rs2512640874 | 19:7,682,251 | G/A | — | likely benign |
| rs754308415 | 19:7,682,262 | G/A | — | uncertain significance |
| rs549080555 | 19:7,682,264 | G/C | — | uncertain significance |
| rs375397200 | 19:7,682,292 | C/T | — | uncertain significance |
| rs754743404 | 19:7,682,300 | C/T | — | uncertain significance |
| rs2030880230 | 19:7,682,521 | G/A | — | uncertain significance |
| rs1301331358 | 19:7,682,717 | T/C | — | uncertain significance |
| rs373173219 | 19:7,682,741 | C/T | — | uncertain significance |
| rs1333171852 | 19:7,682,749 | G/A | — | uncertain significance |
| rs747834400 | 19:7,682,926 | G/A | — | likely benign |
Gene information from NCBI Gene. Variant classifications from ClinVar.