DYNC1I1
dynein cytoplasmic 1 intermediate chain 1
Summary
Enables spectrin binding activity. Involved in vesicle transport along microtubule. Located in several cellular components, including kinetochore; recycling endosome; and spindle pole. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants90 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1842104 | 7:95,413,409 | C/T | — | — |
| rs1315133724 | 7:95,434,070 | A/G | — | uncertain significance |
| rs147587226 | 7:95,434,074 | A/G | — | likely benign |
| rs759131345 | 7:95,434,077 | G/A | — | likely benign |
| rs756972511 | 7:95,434,120 | C/T | — | uncertain significance |
| rs41278809 | 7:95,434,156 | C/G | — | benign |
| rs1060499856 | 7:95,439,697 | C/T | — | likely benign |
| rs76250658 | 7:95,439,735 | A/C | — | benign |
| rs149830072 | 7:95,439,782 | C/T | — | benign |
| rs78122113 | 7:95,439,811 | G/A | — | benign |
| rs757363632 | 7:95,439,828 | A/T | — | likely benign |
| rs117676704 | 7:95,442,510 | C/G | — | benign |
| rs199740432 | 7:95,442,514 | C/T | — | uncertain significance |
| rs145885345 | 7:95,442,629 | C/A | — | likely benign |
| rs2484657831 | 7:95,442,637 | G/C | — | uncertain significance |
| rs1794872908 | 7:95,442,640 | C/T | — | uncertain significance |
| rs1227517 | 7:95,457,160 | C/T | — | benign |
| rs41278815 | 7:95,457,198 | C/T | — | benign |
| rs1227516 | 7:95,457,224 | G/C | — | benign |
| rs41278818 | 7:95,457,256 | G/A | — | benign |
| rs3757696 | 7:95,499,066 | C/A | — | benign |
| rs79162063 | 7:95,499,183 | T/C | — | benign |
| rs3757697 | 7:95,499,234 | A/G | — | benign |
| rs370302761 | 7:95,499,329 | T/C | — | likely benign |
| rs540198998 | 7:95,529,442 | C/T | — | — |
| rs13231718 | 7:95,600,368 | T/G | intron variant | — |
| rs2051706 | 7:95,606,507 | A/T | — | — |
| rs12540849 | 7:95,606,624 | C/A | — | benign |
| rs765771171 | 7:95,606,845 | T/C | — | uncertain significance |
| rs370031174 | 7:95,606,851 | A/G | — | uncertain significance |
| rs35314029 | 7:95,606,877 | C/A | — | benign |
| rs1793341633 | 7:95,606,911 | A/C | — | uncertain significance |
| rs6968143 | 7:95,614,022 | G/C | — | benign |
| rs6967779 | 7:95,614,078 | A/C | — | benign |
| rs752932291 | 7:95,614,165 | A/G | — | uncertain significance |
| rs749647527 | 7:95,614,188 | C/T | — | likely benign |
| rs142927191 | 7:95,614,242 | C/T | — | likely benign |
| rs139485962 | 7:95,614,272 | G/A | — | benign |
| rs55710908 | 7:95,614,396 | G/A | — | benign |
| rs2073984 | 7:95,614,467 | G/T | — | benign |
| rs6950751 | 7:95,614,483 | T/A | — | benign |
| rs17705339 | 7:95,616,309 | T/C | — | benign |
| rs62467724 | 7:95,616,330 | G/A | — | benign |
| rs746551909 | 7:95,616,412 | A/G | — | uncertain significance |
| rs62467742 | 7:95,624,126 | A/G | intron variant | — |
| rs114787302 | 7:95,625,111 | T/C | — | benign |
| rs10265938 | 7:95,625,189 | T/C | — | benign |
| rs371792280 | 7:95,625,271 | G/A | — | likely benign |
| rs771966085 | 7:95,625,313 | A/T | — | uncertain significance |
| rs147131803 | 7:95,625,323 | G/A | — | uncertain significance |
| rs777588095 | 7:95,625,339 | A/G | — | uncertain significance |
| rs188393972 | 7:95,625,370 | C/T | — | likely benign |
| rs148644569 | 7:95,625,371 | G/A | — | uncertain significance |
| rs116104078 | 7:95,625,460 | C/T | — | benign |
| rs1488515 | 7:95,631,196 | T/G | intron variant | — |
| rs2115962402 | 7:95,657,493 | G/C | — | uncertain significance |
| rs201240633 | 7:95,657,501 | G/A | — | benign |
| rs1275980376 | 7:95,661,982 | C/G | — | uncertain significance |
| rs1794843451 | 7:95,662,077 | G/A | — | uncertain significance |
| rs147715816 | 7:95,662,097 | G/A | — | likely benign |
| rs112578229 | 7:95,664,919 | G/A | — | likely benign |
| rs760589743 | 7:95,664,953 | A/G | — | uncertain significance |
| rs867286355 | 7:95,664,954 | T/C | — | likely benign |
| rs375862083 | 7:95,664,970 | G/T | — | uncertain significance |
| rs774000073 | 7:95,665,018 | G/A | — | uncertain significance |
| rs139354581 | 7:95,665,023 | C/T | — | likely benign |
| rs551953723 | 7:95,665,046 | C/T | — | uncertain significance |
| rs2485280427 | 7:95,668,590 | A/G | — | uncertain significance |
| rs1048666 | 7:95,668,664 | C/A | — | benign |
| rs77909595 | 7:95,700,008 | C/G | — | — |
| rs1433585475 | 7:95,705,455 | C/T | — | likely benign |
| rs376956482 | 7:95,705,497 | C/T | — | likely benign |
| rs42083 | 7:95,709,602 | T/C | — | benign |
| rs42082 | 7:95,709,666 | A/C | — | benign |
| rs370341645 | 7:95,709,695 | C/T | — | likely benign |
| rs774678955 | 7:95,709,702 | G/C | — | uncertain significance |
| rs145003989 | 7:95,709,710 | C/T | — | likely benign |
| rs2485437666 | 7:95,709,711 | G/A | — | uncertain significance |
| rs781314687 | 7:95,709,757 | T/C | — | uncertain significance |
| rs1452319389 | 7:95,709,774 | C/T | — | uncertain significance |
| rs774931974 | 7:95,709,782 | G/T | — | uncertain significance |
| rs145694237 | 7:95,709,792 | G/A | — | uncertain significance |
| rs1294951645 | 7:95,709,795 | G/A | — | uncertain significance |
| rs1298576123 | 7:95,726,811 | A/G | — | uncertain significance |
| rs766333170 | 7:95,726,872 | C/T | — | likely benign |
| rs1170868175 | 7:95,726,897 | T/C | — | uncertain significance |
| rs7794344 | 7:95,727,014 | T/C | — | benign |
| rs118137579 | 7:95,728,470 | G/C | downstream gene variant | — |
| rs550636387 | 7:95,739,347 | A/G | — | benign |
| rs185004446 | 7:95,739,389 | T/C | — | benign |
Gene information from NCBI Gene. Variant classifications from ClinVar.