KIF26B

kinesin family member 26B

Summary

The protein encoded by this gene is an intracellular motor protein thought to transport organelles along microtubules. The encoded protein is required for kidney development. Elevated levels of this protein have been found in some breast and colorectal cancers. [provided by RefSeq, Mar 2017]

Known Variants245 total

rsid	Position (GRCh37)	Alleles	Class	ClinVar
rs757922173	1:245,318,746	A/T	—	uncertain significance
rs371147522	1:245,319,602	C/T	—	uncertain significance
rs533597039	1:245,319,691	G/A	—	benign
rs1274965722	1:245,319,695	G/T	—	uncertain significance
rs765071022	1:245,319,742	C/G	—	likely benign
rs762519197	1:245,319,791	G/A	—	uncertain significance
rs772909497	1:245,319,884	G/C	—	uncertain significance
rs1365733099	1:245,319,951	T/C	—	uncertain significance
rs752444847	1:245,319,955	G/T	—	uncertain significance
rs576183812	1:245,319,967	G/C	—	likely benign
rs1158426786	1:245,319,973	C/T	—	likely benign
rs1462081144	1:245,319,978	C/T	—	uncertain significance
rs372237124	1:245,530,149	C/T	—	uncertain significance
rs201717788	1:245,530,177	C/T	—	likely benign
rs371384388	1:245,530,204	C/T	—	likely benign
rs1198485011	1:245,530,252	G/A	—	likely benign
rs745778571	1:245,530,281	C/T	—	uncertain significance
rs372431324	1:245,530,290	A/C	—	uncertain significance
rs753008235	1:245,530,316	G/A	—	uncertain significance
rs369552215	1:245,530,320	C/T	—	uncertain significance
rs745665621	1:245,530,321	G/A	—	likely benign
rs1040080802	1:245,530,343	T/G	—	uncertain significance
rs190637518	1:245,530,446	G/T	—	benign
rs375067079	1:245,530,489	C/T	—	likely benign
rs200520003	1:245,530,546	C/T	—	likely benign
rs114860672	1:245,530,583	A/C	—	likely benign
rs1229507139	1:245,530,644	A/G	—	uncertain significance
rs150921857	1:245,530,645	C/T	—	benign
rs548748856	1:245,550,097	G/A	—	—
rs544985	1:245,575,353	T/A	intron variant	—
rs594672	1:245,575,817	C/T	intron variant	—
rs1069219	1:245,580,406	T/C	intron variant	—
rs1093958	1:245,581,499	A/C	intron variant	—
rs1658422743	1:245,582,901	G/C	—	uncertain significance
rs1284226189	1:245,582,905	A/G	—	likely benign
rs199613431	1:245,582,955	G/A	—	likely benign
rs1405973236	1:245,582,971	G/A	—	uncertain significance
rs937147286	1:245,583,004	G/A	—	uncertain significance
rs148234227	1:245,583,009	T/C	—	benign
rs1178197899	1:245,583,022	T/C	—	uncertain significance
rs1756912	1:245,588,095	G/A	intron variant	—
rs146288131	1:245,616,291	A/G	intron variant	—
rs545247916	1:245,704,074	C/T	—	uncertain significance
rs372632341	1:245,704,092	C/A	—	uncertain significance
rs771571204	1:245,704,113	G/A	—	uncertain significance
rs372159973	1:245,704,129	C/T	—	likely benign
rs61754898	1:245,704,130	G/C	—	likely benign
rs2527914792	1:245,704,166	G/A	—	uncertain significance
rs749730146	1:245,704,217	G/A	—	uncertain significance
rs2103102844	1:245,704,242	G/A	—	uncertain significance
rs375730929	1:245,704,262	T/C	—	likely benign
rs10924245	1:245,733,608	G/T	intron variant	—
rs777339201	1:245,753,479	G/A	—	—
rs576596746	1:245,756,555	T/C	—	—
rs779367297	1:245,765,981	G/A	—	uncertain significance
rs61831269	1:245,766,015	A/G	—	likely benign
rs1490451180	1:245,766,029	C/G	—	uncertain significance
rs746908968	1:245,770,954	C/T	—	uncertain significance
rs113032967	1:245,772,587	C/T	—	likely benign
rs61754955	1:245,772,651	C/G	—	benign
rs61755865	1:245,772,692	A/C	—	benign
rs372844982	1:245,772,707	C/A	—	benign
rs775831302	1:245,772,764	G/A	—	likely benign
rs1030984454	1:245,772,790	C/T	—	uncertain significance
rs149117112	1:245,772,826	C/T	—	benign
rs138313317	1:245,775,163	T/G	—	uncertain significance
rs199839162	1:245,775,183	A/G	—	likely benign
rs752143373	1:245,775,203	G/C	—	uncertain significance
rs149649213	1:245,775,210	G/A	—	uncertain significance
rs2527473724	1:245,775,239	A/G	—	uncertain significance
rs61741293	1:245,775,265	C/T	—	benign
rs144325629	1:245,775,287	A/G	—	benign
rs529486807	1:245,782,519	G/T	—	—
rs10924270	1:245,804,664	A/T	—	—
rs754222042	1:245,809,434	C/T	—	uncertain significance
rs1267523178	1:245,809,447	A/G	—	uncertain significance
rs368743387	1:245,809,460	C/T	—	likely benign
rs2527542661	1:245,809,557	A/C	—	uncertain significance
rs1333605495	1:245,809,560	G/A	—	uncertain significance
rs10802241	1:245,826,657	C/G	intron variant	—
rs2527622907	1:245,847,562	G/A	—	likely benign
rs373588212	1:245,847,587	C/T	—	uncertain significance
rs2527623083	1:245,847,607	C/A	—	uncertain significance
rs1284056538	1:245,847,613	G/A	—	likely benign
rs532973058	1:245,847,616	C/T	—	likely benign
rs199561730	1:245,847,617	G/A	—	uncertain significance
rs61831276	1:245,847,622	T/C	—	benign
rs368623828	1:245,847,632	G/A	—	uncertain significance
rs376018469	1:245,848,724	C/T	—	likely benign
rs200317382	1:245,848,781	C/A	—	likely benign
rs374638007	1:245,848,820	C/T	—	likely benign
rs200467850	1:245,848,821	G/A	—	uncertain significance
rs199690740	1:245,848,890	G/A	—	uncertain significance
rs190318015	1:245,848,940	C/A	—	benign
rs756497702	1:245,848,947	G/A	—	uncertain significance
rs747266335	1:245,848,984	G/A	—	uncertain significance
rs61744484	1:245,848,996	A/G	—	benign
rs61744485	1:245,849,000	C/T	—	benign
rs2527626946	1:245,849,013	G/C	—	uncertain significance
rs371121385	1:245,849,042	C/T	—	likely benign

Showing 100 of 245 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.