BICD2

BICD cargo adaptor 2

Summary

This gene is one of two human homologs of Drosophila bicaudal-D and a member of the Bicoid family. It has been implicated in dynein-mediated, minus end-directed motility along microtubules. It has also been reported to be a phosphorylation target of NIMA related kinase 8. Two alternative splice variants have been described. [provided by RefSeq, Jul 2008]

Known Variants723 total

rsid	Position (GRCh37)	Alleles	Class	ClinVar
rs10992429	9:95,475,647	G/T	—	benign
rs3739605	9:95,475,937	G/A	—	benign
rs7862106	9:95,476,441	C/G	3 prime UTR variant	—
rs76331256	9:95,477,300	C/T	—	likely benign
rs528694770	9:95,477,416	C/T	—	likely benign
rs2490433638	9:95,477,441	C/T	—	uncertain significance
rs2490433651	9:95,477,445	G/A	—	likely benign
rs1853276595	9:95,477,457	C/A	—	uncertain significance
rs1412613776	9:95,477,459	T/G	—	uncertain significance
rs533026038	9:95,477,460	C/T	—	benign
rs766447651	9:95,477,462	C/T	—	uncertain significance
rs775345022	9:95,477,463	G/A	—	benign
rs760624844	9:95,477,468	A/G	—	likely benign
rs763836233	9:95,477,477	G/A	—	uncertain significance
rs756910200	9:95,477,489	C/T	—	conflicting classifications of pathogenicity
rs144390290	9:95,477,490	G/A	—	likely benign
rs757915845	9:95,477,494	C/A	—	uncertain significance
rs779724776	9:95,477,498	C/T	—	likely benign
rs566505973	9:95,477,499	G/A	—	likely benign
rs755577434	9:95,477,504	T/C	—	likely benign
rs146163062	9:95,477,507	C/T	—	likely benign
rs201354084	9:95,477,508	G/A	—	likely benign
rs2490433866	9:95,477,511	G/A	—	likely benign
rs1853278571	9:95,477,519	C/T	—	uncertain significance
rs777787730	9:95,477,523	G/C	—	likely benign
rs971599943	9:95,477,525	T/C	—	likely benign
rs774445661	9:95,477,534	C/G	—	uncertain significance
rs199989045	9:95,477,535	G/A	—	benign
rs1853279588	9:95,477,536	C/T	—	uncertain significance
rs768524403	9:95,477,539	G/A	—	uncertain significance
rs776472510	9:95,477,543	T/C	—	conflicting classifications of pathogenicity
rs200341779	9:95,477,552	T/C	—	likely benign
rs34451610	9:95,477,559	C/T	—	likely benign
rs762717269	9:95,477,560	G/A	—	conflicting classifications of pathogenicity
rs751158467	9:95,477,564	C/T	—	uncertain significance
rs755522406	9:95,477,565	G/A	—	likely benign
rs2490434102	9:95,477,573	C/T	—	uncertain significance
rs556905704	9:95,477,575	C/T	—	likely benign
rs778218322	9:95,477,576	G/A	—	uncertain significance
rs372322527	9:95,477,581	C/T	—	likely benign
rs143189118	9:95,477,582	G/A	—	uncertain significance
rs1564057942	9:95,477,584	C/T	—	uncertain significance
rs778940849	9:95,477,585	G/A	—	uncertain significance
rs768632390	9:95,477,592	C/T	—	likely benign
rs776367463	9:95,477,603	G/A	—	likely benign
rs1273239213	9:95,477,606	C/T	—	uncertain significance
rs151133287	9:95,477,607	G/A	—	likely benign
rs140205029	9:95,477,618	G/A	—	likely benign
rs1473987839	9:95,477,620	C/T	—	uncertain significance
rs756421767	9:95,477,621	G/A	—	uncertain significance
rs572517685	9:95,477,631	C/T	—	likely benign
rs1853283714	9:95,477,632	G/C	—	uncertain significance
rs1382501486	9:95,477,634	C/T	—	likely benign
rs200816999	9:95,477,636	G/A	—	conflicting classifications of pathogenicity
rs759037874	9:95,477,640	C/T	—	likely benign
rs2131496275	9:95,477,646	G/T	—	likely benign
rs1853284222	9:95,477,649	G/A	—	likely benign
rs149891938	9:95,477,654	T/C	—	likely benign
rs144944522	9:95,477,657	G/A	—	uncertain significance
rs754249319	9:95,477,664	C/T	—	likely benign
rs377454040	9:95,477,665	G/A	—	conflicting classifications of pathogenicity
rs950657224	9:95,477,670	C/T	—	likely benign
rs779170531	9:95,477,673	C/T	—	conflicting classifications of pathogenicity
rs1587666004	9:95,477,675	T/C	—	uncertain significance
rs2131496327	9:95,477,677	T/G	—	uncertain significance
rs398123030	9:95,477,683	T/C	missense variant	pathogenic
rs1131691347	9:95,477,684	C/T	—	pathogenic
rs370848787	9:95,477,685	G/A	—	likely benign
rs2490434765	9:95,477,690	C/T	—	uncertain significance
rs561748013	9:95,477,691	A/T	—	benign
rs573705109	9:95,477,697	C/T	—	likely benign
rs773121830	9:95,477,698	G/A	—	uncertain significance
rs1357621526	9:95,477,703	C/T	—	likely benign
rs1216459221	9:95,477,707	C/T	—	uncertain significance
rs587777889	9:95,477,708	G/A	—	benign
rs1853288308	9:95,477,710	T/C	—	uncertain significance
rs1853288605	9:95,477,719	T/A	—	uncertain significance
rs766894803	9:95,477,732	T/C	—	uncertain significance
rs751036331	9:95,477,739	G/A	—	likely benign
rs921619761	9:95,477,745	C/T	—	likely benign
rs2490434950	9:95,477,748	G/A	—	uncertain significance
rs199833926	9:95,477,764	T/C	—	likely benign
rs10992430	9:95,477,951	G/T	—	benign
rs115497220	9:95,478,030	C/T	—	likely benign
rs111836891	9:95,479,785	C/T	—	likely benign
rs116139949	9:95,479,978	C/T	—	likely benign
rs376177099	9:95,480,061	C/G	—	likely benign
rs554612134	9:95,480,062	G/C	—	likely benign
rs140501870	9:95,480,064	C/G	—	likely benign
rs1200601940	9:95,480,065	A/G	—	likely benign
rs929825881	9:95,480,068	A/G	—	likely benign
rs750839993	9:95,480,072	C/T	—	likely benign
rs566572599	9:95,480,073	G/A	—	conflicting classifications of pathogenicity
rs145923602	9:95,480,092	T/C	—	conflicting classifications of pathogenicity
rs878944571	9:95,480,097	C/A	—	conflicting classifications of pathogenicity
rs1587667544	9:95,480,098	G/A	—	conflicting classifications of pathogenicity
rs373990508	9:95,480,102	C/A	—	likely benign
rs781440350	9:95,480,103	G/A	—	uncertain significance
rs1064793875	9:95,480,106	G/A	missense variant	pathogenic
rs1853348980	9:95,480,108	G/A	—	likely benign

Showing 100 of 723 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.