EXOC3L4
exocyst complex component 3 like 4
Summary
Predicted to enable SNARE binding activity. Predicted to be involved in exocyst localization and exocytosis. Predicted to be part of exocyst. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants86 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs74085382 | 14:103,560,996 | A/G | — | — |
| rs150110852 | 14:103,561,553 | G/A | upstream gene variant | — |
| rs8017161 | 14:103,563,195 | G/A | upstream gene variant | — |
| rs150640215 | 14:103,563,237 | T/A | upstream gene variant | — |
| rs11628185 | 14:103,563,421 | G/A | upstream gene variant | — |
| rs143155265 | 14:103,564,278 | C/T | upstream gene variant | — |
| rs59643720 | 14:103,564,807 | A/G | — | — |
| rs17101241 | 14:103,564,820 | A/G | — | — |
| rs61462345 | 14:103,564,935 | C/T | — | — |
| rs56956502 | 14:103,565,044 | G/A | coding sequence variant | — |
| rs62006947 | 14:103,565,370 | A/T | — | — |
| rs545706151 | 14:103,565,961 | C/T | — | — |
| rs2297067 | 14:103,566,785 | C/T | missense variant | — |
| rs781292802 | 14:103,566,810 | G/A | — | uncertain significance |
| rs373963350 | 14:103,566,818 | C/T | — | uncertain significance |
| rs138581876 | 14:103,566,853 | T/G | — | likely benign |
| rs767985118 | 14:103,566,914 | A/G | — | uncertain significance |
| rs138887682 | 14:103,568,488 | G/A | missense variant | — |
| rs1318284277 | 14:103,568,538 | G/C | — | uncertain significance |
| rs370099239 | 14:103,568,587 | C/G | — | uncertain significance |
| rs766530029 | 14:103,568,621 | C/G | — | uncertain significance |
| rs1268635683 | 14:103,568,653 | G/T | — | uncertain significance |
| rs763372631 | 14:103,568,707 | G/A | — | uncertain significance |
| rs10142200 | 14:103,568,729 | A/G | synonymous variant | — |
| rs778716701 | 14:103,568,742 | C/A | — | uncertain significance |
| rs10142287 | 14:103,568,747 | C/G | — | benign |
| rs770174979 | 14:103,568,749 | A/G | — | uncertain significance |
| rs2503860348 | 14:103,568,775 | C/A | — | uncertain significance |
| rs1370140490 | 14:103,568,796 | G/C | — | uncertain significance |
| rs902650716 | 14:103,568,836 | G/T | — | uncertain significance |
| rs1161131288 | 14:103,568,877 | T/A | — | uncertain significance |
| rs9324055 | 14:103,568,949 | G/A | — | benign |
| rs139497928 | 14:103,568,953 | A/T | missense variant | — |
| rs1017107033 | 14:103,568,978 | C/G | — | uncertain significance |
| rs1454447335 | 14:103,568,983 | C/T | — | uncertain significance |
| rs369448990 | 14:103,568,991 | G/A | — | uncertain significance |
| rs919870195 | 14:103,569,001 | G/A | — | uncertain significance |
| rs1372052652 | 14:103,569,006 | T/G | — | uncertain significance |
| rs373971768 | 14:103,569,028 | G/A | — | uncertain significance |
| rs751477109 | 14:103,569,039 | C/T | — | uncertain significance |
| rs72706640 | 14:103,569,748 | T/C | regulatory region variant | — |
| rs151184170 | 14:103,570,132 | C/T | — | — |
| rs147121761 | 14:103,570,134 | C/T | — | — |
| rs2503879592 | 14:103,570,301 | G/A | — | uncertain significance |
| rs117708804 | 14:103,570,354 | G/T | — | benign |
| rs769119664 | 14:103,570,378 | A/C | — | uncertain significance |
| rs572934887 | 14:103,570,385 | T/C | — | uncertain significance |
| rs2503885546 | 14:103,570,682 | C/A | — | uncertain significance |
| rs373755145 | 14:103,570,694 | T/C | — | uncertain significance |
| rs1162977128 | 14:103,570,718 | G/A | — | uncertain significance |
| rs2503891436 | 14:103,571,096 | G/A | — | uncertain significance |
| rs968745964 | 14:103,571,160 | G/A | — | uncertain significance |
| rs773363855 | 14:103,571,357 | G/C | — | uncertain significance |
| rs78702790 | 14:103,571,837 | G/C | regulatory region variant | — |
| rs7150997 | 14:103,571,874 | C/A | — | — |
| rs944002 | 14:103,572,815 | A/G | intron variant | — |
| rs2503913232 | 14:103,573,786 | G/A | — | likely benign |
| rs568450369 | 14:103,573,813 | A/G | — | likely benign |
| rs150993709 | 14:103,573,842 | G/A | — | likely benign |
| rs147895517 | 14:103,573,866 | C/T | — | uncertain significance |
| rs147044211 | 14:103,573,873 | G/A | — | uncertain significance |
| rs759676549 | 14:103,573,995 | G/A | — | uncertain significance |
| rs1000855439 | 14:103,574,038 | G/A | — | uncertain significance |
| rs773079020 | 14:103,574,043 | C/T | — | likely benign |
| rs1340829630 | 14:103,574,060 | G/T | — | uncertain significance |
| rs1448975984 | 14:103,574,114 | G/C | — | uncertain significance |
| rs1001363898 | 14:103,574,745 | A/G | — | uncertain significance |
| rs777326406 | 14:103,574,769 | T/C | — | uncertain significance |
| rs757105801 | 14:103,574,790 | G/A | — | uncertain significance |
| rs756097471 | 14:103,574,803 | A/G | — | uncertain significance |
| rs549171249 | 14:103,574,814 | C/T | — | uncertain significance |
| rs149136706 | 14:103,575,521 | T/C | regulatory region variant | — |
| rs145260258 | 14:103,575,524 | C/T | regulatory region variant | — |
| rs200884137 | 14:103,576,369 | C/T | missense variant | — |
| rs770577262 | 14:103,576,394 | C/A | — | uncertain significance |
| rs767477397 | 14:103,576,409 | G/C | — | uncertain significance |
| rs780276149 | 14:103,576,412 | G/A | — | uncertain significance |
| rs537049883 | 14:103,576,418 | G/A | — | uncertain significance |
| rs777178744 | 14:103,576,421 | A/C | — | uncertain significance |
| rs367579528 | 14:103,576,427 | A/G | — | likely benign |
| rs744153 | 14:103,576,444 | C/A | missense variant | — |
| rs762956732 | 14:103,576,445 | A/G | — | uncertain significance |
| rs544292874 | 14:103,576,468 | G/A | — | uncertain significance |
| rs766420697 | 14:103,576,496 | G/A | — | uncertain significance |
| rs368633703 | 14:103,576,499 | G/T | — | uncertain significance |
| rs557001430 | 14:103,576,540 | G/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.