ZNF778

zinc finger protein 778

Summary

The protein encoded by this gene is a member of the krueppel C2H2-type zinc-finger protein family, and it contains one KRAB domain and eighteen C2H2-type zinc fingers. This gene is a candidate gene for autism and variable cognitive impairment in the 16q24.3 microdeletion syndrome. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Jan 2011]

Known Variants105 total

rsidPosition (GRCh37)AllelesClassClinVar
rs14765371116:89,272,599C/A——
rs77408875916:89,273,124A/G——
rs137211604616:89,287,554G/A—uncertain significance
rs254405191416:89,288,519C/G—uncertain significance
rs76254362616:89,288,526T/G—uncertain significance
rs20152895816:89,288,548A/G—likely benign
rs203102196616:89,288,590A/G—uncertain significance
rs78175619316:89,289,571G/A—uncertain significance
rs56577254016:89,289,586G/A—uncertain significance
rs37735275316:89,289,620T/C—uncertain significance
rs148683515816:89,291,134C/G—uncertain significance
rs15083061716:89,291,157A/G—benign
rs135428724416:89,291,169A/G—uncertain significance
rs20166240016:89,291,969G/A—uncertain significance
rs75718817016:89,291,996G/A—uncertain significance
rs119039366316:89,292,019G/A—likely benign
rs37728036316:89,292,032C/T—uncertain significance
rs57039511316:89,292,934G/C——
rs104255385516:89,293,105A/G—uncertain significance
rs77295498016:89,293,162G/A—uncertain significance
rs103016369716:89,293,174C/G—uncertain significance
rs75276044316:89,293,186G/A—uncertain significance
rs20116466316:89,293,202C/T—uncertain significance
rs76939275316:89,293,204G/C—uncertain significance
rs203151203716:89,293,223A/C—uncertain significance
rs19155555916:89,293,303T/C—uncertain significance
rs37022025116:89,293,348G/A—likely benign
rs18342397016:89,293,354A/G—uncertain significance
rs76192756816:89,293,358G/A—uncertain significance
rs18800849016:89,293,369C/G—uncertain significance
rs19963988816:89,293,388G/C—uncertain significance
rs14908063416:89,293,423C/Tmissense variant—
rs76318310516:89,293,424G/A—uncertain significance
rs57514143916:89,293,465C/A—uncertain significance
rs76984083416:89,293,466C/T—uncertain significance
rs8023184216:89,293,524C/T—benign
rs53345771116:89,293,540G/A—uncertain significance
rs37751618716:89,293,550A/C—uncertain significance
rs53108758616:89,293,574C/G—uncertain significance
rs18387029716:89,293,592G/T—uncertain significance
rs77017183916:89,293,621T/A—uncertain significance
rs117634307216:89,293,652C/G—uncertain significance
rs20104120216:89,293,661C/T—uncertain significance
rs19963617016:89,293,691C/A—uncertain significance
rs254406795116:89,293,692T/C—likely benign
rs127714721116:89,293,696G/A—uncertain significance
rs53203288416:89,293,723G/A—uncertain significance
rs137797003716:89,293,781A/G—uncertain significance
rs36791873016:89,293,786C/T—uncertain significance
rs36888249816:89,293,790A/G—uncertain significance
rs37348566716:89,293,829A/G—uncertain significance
rs74766383816:89,293,844A/G—uncertain significance
rs77420842316:89,293,856A/G—likely benign
rs20013011916:89,293,891G/A—uncertain significance
rs37724327016:89,293,968C/G—uncertain significance
rs77181766916:89,293,979A/G—uncertain significance
rs36868633416:89,293,987A/G—uncertain significance
rs13901992816:89,293,993C/T—uncertain significance
rs19039997016:89,293,994G/A—uncertain significance
rs76202672716:89,293,997G/A—uncertain significance
rs75206677416:89,294,009G/A—uncertain significance
rs77852167516:89,294,018G/A—uncertain significance
rs19996502316:89,294,027C/T—uncertain significance
rs57300033816:89,294,032G/A—uncertain significance
rs18175574516:89,294,059G/A—uncertain significance
rs131879192716:89,294,086C/G—uncertain significance
rs254406953516:89,294,089A/G—uncertain significance
rs18509678916:89,294,111C/G—uncertain significance
rs156750662316:89,294,150C/G—uncertain significance
rs54318159216:89,294,174C/T—uncertain significance
rs37104689016:89,294,245C/T—uncertain significance
rs18108177016:89,294,246G/A—uncertain significance
rs77907693516:89,294,258C/A—uncertain significance
rs75859341516:89,294,266A/G—uncertain significance
rs136983453116:89,294,267T/C—likely benign
rs14637028316:89,294,280C/T—benign
rs37162225216:89,294,281G/A—uncertain significance
rs37564164616:89,294,305G/C—uncertain significance
rs75178875616:89,294,324A/G—uncertain significance
rs75525906316:89,294,326A/T—uncertain significance
rs96492165416:89,294,363C/T—uncertain significance
rs37580669416:89,294,417C/T—uncertain significance
rs18521856116:89,294,418G/A—likely benign
rs76635328516:89,294,437C/G—uncertain significance
rs156750764916:89,294,467T/C—uncertain significance
rs131515342516:89,294,472G/C—uncertain significance
rs76233142316:89,294,522G/A—uncertain significance
rs76087364216:89,294,590C/T—uncertain significance
rs54455127716:89,294,596G/A—uncertain significance
rs56284609616:89,294,617G/A—uncertain significance
rs36785357116:89,294,743C/T—uncertain significance
rs54780073716:89,294,794C/A—uncertain significance
rs77922345816:89,294,801A/C—uncertain significance
rs52740682116:89,294,818A/C—uncertain significance
rs203170124116:89,294,832G/T—uncertain significance
rs19987888416:89,294,893G/C—uncertain significance
rs54974778016:89,294,903A/C—uncertain significance
rs37495020416:89,294,933A/G—uncertain significance
rs19139460016:89,296,647G/Aregulatory region variant—
rs56422173716:89,299,382T/C—likely benign

Showing 100 of 105 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.