WWC1
WW and C2 domain containing 1
Summary
The protein encoded by this gene is a cytoplasmic phosphoprotein that interacts with PRKC-zeta and dynein light chain-1. Alleles of this gene have been found that enhance memory in some individuals. Three transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Mar 2010]
Known Variants93 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs375703595 | 5:167,719,152 | G/A | — | likely benign |
| rs370421132 | 5:167,719,153 | G/A | — | likely benign |
| rs755080861 | 5:167,719,177 | C/G | — | uncertain significance |
| rs535312961 | 5:167,719,204 | G/A | — | uncertain significance |
| rs2537343629 | 5:167,719,243 | A/G | — | likely benign |
| rs2537343814 | 5:167,719,264 | A/G | — | uncertain significance |
| rs13164530 | 5:167,724,186 | G/T | intron variant | — |
| rs147106204 | 5:167,741,566 | C/A | intron variant | — |
| rs6555802 | 5:167,773,074 | A/T | — | — |
| rs11740112 | 5:167,778,773 | G/A | intron variant | — |
| rs10475878 | 5:167,790,204 | G/A | intron variant | — |
| rs6555805 | 5:167,797,440 | C/T | intron variant | — |
| rs13171394 | 5:167,807,992 | G/A | intron variant | — |
| rs755813 | 5:167,809,693 | G/A | — | — |
| rs4320284 | 5:167,811,567 | T/A | — | — |
| rs557621965 | 5:167,812,255 | G/A | — | uncertain significance |
| rs1272460272 | 5:167,833,235 | G/C | — | uncertain significance |
| rs1255526670 | 5:167,833,294 | A/C | — | uncertain significance |
| rs2241368 | 5:167,835,390 | A/G | intron variant | — |
| rs201637507 | 5:167,835,513 | G/A | — | uncertain significance |
| rs765217357 | 5:167,835,521 | A/G | — | uncertain significance |
| rs370191617 | 5:167,835,533 | G/A | — | uncertain significance |
| rs17551608 | 5:167,835,539 | C/T | missense variant | benign |
| rs114682488 | 5:167,835,629 | G/A | — | benign |
| rs1481393288 | 5:167,836,948 | C/A | — | uncertain significance |
| rs750305410 | 5:167,841,361 | A/T | — | uncertain significance |
| rs1243803274 | 5:167,841,413 | G/T | — | likely benign |
| rs933956190 | 5:167,841,445 | A/T | — | uncertain significance |
| rs201176909 | 5:167,841,484 | G/T | — | uncertain significance |
| rs1276099603 | 5:167,841,517 | A/G | — | uncertain significance |
| rs200207821 | 5:167,841,564 | C/A | — | benign |
| rs4976602 | 5:167,843,998 | G/A | intron variant | — |
| rs2003850 | 5:167,844,095 | C/A | — | — |
| rs729387 | 5:167,844,571 | A/G | intron variant | — |
| rs17070145 | 5:167,845,791 | C/T | intron variant | association |
| rs11134512 | 5:167,847,460 | T/G | intron variant | — |
| rs145003784 | 5:167,849,049 | A/G | — | likely benign |
| rs1781285252 | 5:167,850,563 | T/A | — | uncertain significance |
| rs142973533 | 5:167,850,734 | G/A | — | benign |
| rs147044558 | 5:167,850,740 | C/T | — | uncertain significance |
| rs763165879 | 5:167,850,753 | G/A | — | uncertain significance |
| rs2532917159 | 5:167,850,792 | A/C | — | uncertain significance |
| rs755958353 | 5:167,850,812 | C/T | — | uncertain significance |
| rs139884736 | 5:167,850,877 | C/T | — | likely benign |
| rs760218601 | 5:167,851,016 | G/A | — | likely benign |
| rs374015526 | 5:167,851,023 | A/G | — | uncertain significance |
| rs199869735 | 5:167,851,031 | C/T | — | uncertain significance |
| rs758480535 | 5:167,851,032 | G/A | — | uncertain significance |
| rs9686714 | 5:167,853,274 | T/A | — | — |
| rs766146003 | 5:167,855,091 | G/A | — | uncertain significance |
| rs146570615 | 5:167,855,129 | C/T | — | benign |
| rs386352379 | 5:167,855,133 | G/A | — | uncertain significance |
| rs116010648 | 5:167,855,138 | C/T | — | benign |
| rs374770777 | 5:167,855,768 | C/T | — | uncertain significance |
| rs148388652 | 5:167,858,265 | G/A | — | uncertain significance |
| rs199667456 | 5:167,858,319 | C/G | — | uncertain significance |
| rs992719274 | 5:167,858,351 | G/A | — | uncertain significance |
| rs3822659 | 5:167,858,372 | T/G | missense variant | — |
| rs372137293 | 5:167,868,720 | C/T | — | uncertain significance |
| rs749653075 | 5:167,868,721 | G/A | — | uncertain significance |
| rs772425970 | 5:167,868,742 | G/A | — | uncertain significance |
| rs779882115 | 5:167,868,759 | A/G | — | uncertain significance |
| rs370600135 | 5:167,868,763 | A/G | — | uncertain significance |
| rs1204905941 | 5:167,868,768 | T/C | — | uncertain significance |
| rs776384154 | 5:167,868,776 | G/T | — | uncertain significance |
| rs368809170 | 5:167,868,816 | C/T | — | uncertain significance |
| rs746212759 | 5:167,868,825 | G/A | — | uncertain significance |
| rs570644950 | 5:167,868,838 | C/T | — | uncertain significance |
| rs372805650 | 5:167,871,502 | G/T | — | uncertain significance |
| rs1164394649 | 5:167,871,589 | T/A | — | uncertain significance |
| rs148648959 | 5:167,880,997 | C/T | — | benign |
| rs976662242 | 5:167,881,002 | C/T | — | uncertain significance |
| rs756618752 | 5:167,881,010 | G/A | — | uncertain significance |
| rs1756081976 | 5:167,881,077 | C/A | — | uncertain significance |
| rs369883223 | 5:167,882,392 | C/G | — | uncertain significance |
| rs146212755 | 5:167,882,425 | G/A | — | uncertain significance |
| rs2533202340 | 5:167,882,507 | G/C | — | uncertain significance |
| rs777792685 | 5:167,882,509 | G/A | — | uncertain significance |
| rs758463069 | 5:167,882,517 | G/A | — | uncertain significance |
| rs780161974 | 5:167,882,524 | G/A | — | uncertain significance |
| rs10038727 | 5:167,886,537 | G/A | intron variant | — |
| rs4576167 | 5:167,886,697 | G/C | intron variant | — |
| rs10040267 | 5:167,888,631 | G/C | — | — |
| rs750795143 | 5:167,891,755 | C/T | — | uncertain significance |
| rs758987247 | 5:167,891,756 | G/A | — | uncertain significance |
| rs576075685 | 5:167,891,761 | G/A | — | uncertain significance |
| rs147393968 | 5:167,891,764 | C/T | — | uncertain significance |
| rs777240715 | 5:167,891,771 | T/C | — | uncertain significance |
| rs140696898 | 5:167,891,932 | C/T | — | uncertain significance |
| rs138122885 | 5:167,891,933 | G/A | — | uncertain significance |
| rs12514426 | 5:167,893,708 | G/A | intron variant | — |
| rs1322781353 | 5:167,894,847 | G/A | — | likely benign |
| rs749318706 | 5:167,894,854 | C/T | stop gained | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.