TENM4

teneurin transmembrane protein 4

Summary

The protein encoded by this gene plays a role in establishing proper neuronal connectivity during development. Defects in this gene have been associated with hereditary essential tremor-5. [provided by RefSeq, Oct 2016]

Known Variants358 total

rsid	Position (GRCh37)	Alleles	Class	ClinVar
rs377035207	11:78,369,150	C/T	—	uncertain significance
rs2497304422	11:78,369,155	T/C	—	uncertain significance
rs938188545	11:78,369,177	C/T	—	uncertain significance
rs61740576	11:78,369,202	G/A	—	likely benign
rs1590916407	11:78,369,212	A/C	—	uncertain significance
rs185503085	11:78,369,215	C/T	—	likely benign
rs779399051	11:78,369,261	G/A	—	uncertain significance
rs117724179	11:78,369,298	G/A	—	likely benign
rs762798194	11:78,369,314	C/T	—	uncertain significance
rs200759241	11:78,369,348	G/A	—	uncertain significance
rs761318240	11:78,369,383	G/A	—	uncertain significance
rs114114492	11:78,369,402	C/T	—	benign
rs34562198	11:78,369,403	G/A	—	likely benign
rs2497307057	11:78,369,411	G/A	—	uncertain significance
rs78572681	11:78,369,413	T/C	—	likely benign
rs1460106951	11:78,369,429	G/A	—	uncertain significance
rs184305763	11:78,369,474	C/T	—	uncertain significance
rs76975254	11:78,369,480	C/T	—	benign
rs764458923	11:78,369,485	T/C	—	uncertain significance
rs114100394	11:78,369,500	C/T	—	benign
rs200437630	11:78,369,501	G/A	—	uncertain significance
rs75922333	11:78,369,573	C/T	—	uncertain significance
rs745533143	11:78,369,591	G/C	—	uncertain significance
rs202241833	11:78,369,597	T/A	—	uncertain significance
rs374802257	11:78,369,633	C/T	—	uncertain significance
rs188600631	11:78,369,650	T/C	—	uncertain significance
rs61745704	11:78,369,684	C/A	—	benign
rs368515496	11:78,369,699	A/G	—	uncertain significance
rs761241041	11:78,369,709	C/G	—	uncertain significance
rs759485865	11:78,369,721	T/G	—	likely benign
rs368080294	11:78,369,727	G/A	—	likely benign
rs376296325	11:78,369,801	G/A	—	uncertain significance
rs200705126	11:78,369,834	G/T	—	benign
rs199816257	11:78,369,856	G/C	—	uncertain significance
rs2277277	11:78,372,536	A/G	—	benign
rs748314290	11:78,372,541	C/T	—	uncertain significance
rs766448601	11:78,372,571	G/T	—	uncertain significance
rs776642107	11:78,372,582	C/T	—	uncertain significance
rs1256512694	11:78,379,986	C/T	—	uncertain significance
rs199909021	11:78,380,078	G/A	—	conflicting classifications of pathogenicity
rs372540311	11:78,380,128	T/A	—	uncertain significance
rs61745709	11:78,380,199	C/T	—	benign
rs189655072	11:78,380,244	G/A	—	likely benign
rs768199920	11:78,380,255	G/T	—	uncertain significance
rs374842734	11:78,380,280	A/G	—	likely benign
rs17136977	11:78,380,328	A/G	—	benign
rs376842336	11:78,380,424	C/T	—	likely benign
rs2497358805	11:78,380,476	C/T	—	uncertain significance
rs375613256	11:78,380,492	C/T	—	uncertain significance
rs1253592523	11:78,380,495	G/A	—	uncertain significance
rs764728212	11:78,380,507	C/G	—	uncertain significance
rs543741690	11:78,380,515	C/T	—	uncertain significance
rs750652207	11:78,380,516	G/A	—	uncertain significance
rs754703622	11:78,380,537	C/T	—	uncertain significance
rs2497359759	11:78,380,591	C/T	—	uncertain significance
rs2497359880	11:78,380,599	C/T	—	uncertain significance
rs555843468	11:78,380,639	C/T	—	uncertain significance
rs186319631	11:78,380,645	C/T	—	uncertain significance
rs370470074	11:78,380,650	C/T	—	uncertain significance
rs758333727	11:78,380,651	G/A	—	uncertain significance
rs1193250974	11:78,380,659	C/T	—	uncertain significance
rs2135669863	11:78,380,681	G/A	—	likely benign
rs561808396	11:78,380,692	C/T	—	uncertain significance
rs372549247	11:78,380,701	T/C	—	uncertain significance
rs950098538	11:78,380,722	A/G	—	uncertain significance
rs61747204	11:78,380,739	G/A	—	benign
rs755853085	11:78,380,755	A/T	—	uncertain significance
rs199514320	11:78,380,756	G/A	—	uncertain significance
rs761633956	11:78,380,818	C/T	—	uncertain significance
rs745950858	11:78,380,866	C/T	—	uncertain significance
rs767570583	11:78,380,902	A/G	—	uncertain significance
rs367616110	11:78,381,004	T/C	—	uncertain significance
rs201663167	11:78,381,036	C/T	—	likely benign
rs1228259831	11:78,381,058	T/A	—	uncertain significance
rs199597334	11:78,381,067	T/C	—	uncertain significance
rs752288267	11:78,381,092	C/T	—	uncertain significance
rs376915445	11:78,381,121	C/T	—	uncertain significance
rs1447189784	11:78,381,152	G/A	—	uncertain significance
rs139879711	11:78,381,156	G/A	—	likely benign
rs556415271	11:78,381,161	C/A	—	uncertain significance
rs776563835	11:78,381,164	T/C	—	uncertain significance
rs61742000	11:78,381,276	T/C	—	benign
rs2497365914	11:78,381,277	G/A	—	uncertain significance
rs376416432	11:78,381,279	C/T	—	likely benign
rs370873891	11:78,381,280	G/A	—	uncertain significance
rs61740650	11:78,381,285	G/A	—	benign
rs1275486193	11:78,381,316	T/C	—	uncertain significance
rs370572793	11:78,381,322	G/A	—	uncertain significance
rs2497366414	11:78,381,352	T/C	—	uncertain significance
rs778605809	11:78,381,376	C/T	—	uncertain significance
rs377317773	11:78,381,473	C/A	—	uncertain significance
rs199958891	11:78,381,481	C/T	—	uncertain significance
rs1477177653	11:78,381,568	C/T	—	uncertain significance
rs192931562	11:78,381,581	G/C	—	benign
rs373347923	11:78,383,138	G/A	—	likely benign
rs1275666406	11:78,383,139	C/A	—	uncertain significance
rs1290042781	11:78,383,145	T/C	—	uncertain significance
rs370993371	11:78,383,156	C/T	—	uncertain significance
rs377174822	11:78,383,218	C/T	—	uncertain significance
rs199973967	11:78,383,259	G/C	—	conflicting classifications of pathogenicity

Showing 100 of 358 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.