TNR

tenascin R

Summary

This gene encodes a member of the tenascin family of extracellular matrix glycoproteins. The encoded protein is restricted to the central nervous system. The protein may play a role in neurite outgrowth, neural cell adhesion and modulation of sodium channel function. It is a constituent of perineuronal nets. [provided by RefSeq, Aug 2013]

Known Variants158 total

rsid	Position (GRCh37)	Alleles	Class	ClinVar
rs146697271	1:175,287,836	G/T	3 prime UTR variant	—
rs200613814	1:175,292,533	C/T	—	uncertain significance
rs768619309	1:175,292,537	G/C	—	uncertain significance
rs1191117184	1:175,292,611	C/T	—	uncertain significance
rs565736776	1:175,293,512	C/T	—	uncertain significance
rs199853947	1:175,293,533	T/G	—	pathogenic
rs778628919	1:175,293,536	G/T	—	likely benign
rs112885396	1:175,293,570	C/T	—	benign
rs1479357103	1:175,293,571	G/A	—	uncertain significance
rs570797805	1:175,293,629	G/A	—	uncertain significance
rs3766680	1:175,296,448	T/C	intron variant	—
rs370406157	1:175,299,211	C/T	—	likely benign
rs755976915	1:175,299,234	T/G	—	likely benign
rs35421365	1:175,299,249	G/A	—	benign
rs201550383	1:175,299,289	G/A	—	likely benign
rs887432545	1:175,299,306	C/T	—	uncertain significance
rs148567170	1:175,299,311	C/T	—	uncertain significance
rs369471259	1:175,304,868	C/T	—	uncertain significance
rs2526232005	1:175,304,870	T/C	—	uncertain significance
rs1571308125	1:175,304,904	G/A	—	pathogenic
rs376896107	1:175,304,918	T/A	—	uncertain significance
rs35332088	1:175,304,941	T/C	—	likely benign
rs148934644	1:175,305,218	T/C	downstream gene variant	—
rs1352878852	1:175,306,684	T/C	—	uncertain significance
rs61731114	1:175,306,758	G/A	—	benign
rs753652754	1:175,323,539	C/T	—	uncertain significance
rs1235446393	1:175,323,551	T/C	—	uncertain significance
rs1571329071	1:175,323,552	G/C	—	uncertain significance
rs544150406	1:175,323,554	T/C	—	uncertain significance
rs2526280362	1:175,323,565	G/T	—	uncertain significance
rs35460270	1:175,323,594	G/A	—	benign
rs562502844	1:175,323,634	G/T	—	conflicting classifications of pathogenicity
rs1055884416	1:175,323,635	T/A	—	uncertain significance
rs201888946	1:175,324,650	C/T	—	uncertain significance
rs775043609	1:175,324,653	C/T	—	uncertain significance
rs999980414	1:175,324,674	C/T	—	likely benign
rs759027372	1:175,324,695	T/C	—	uncertain significance
rs112668786	1:175,324,717	G/A	—	benign
rs1228236510	1:175,325,485	T/C	—	uncertain significance
rs148153913	1:175,325,516	G/A	—	benign
rs112059746	1:175,325,553	C/T	—	likely benign
rs1351898155	1:175,325,582	G/A	—	likely benign
rs139871740	1:175,325,586	G/A	—	uncertain significance
rs764383442	1:175,328,772	C/T	—	uncertain significance
rs1396814891	1:175,328,811	G/T	—	uncertain significance
rs142726733	1:175,328,843	A/G	—	likely benign
rs1226105224	1:175,328,864	A/G	—	uncertain significance
rs778676263	1:175,331,813	G/A	—	uncertain significance
rs61731107	1:175,331,822	C/G	—	benign
rs546435742	1:175,331,871	C/T	—	uncertain significance
rs755988969	1:175,331,880	G/T	—	uncertain significance
rs76938240	1:175,331,892	T/C	—	likely benign
rs2526304059	1:175,331,933	T/G	—	uncertain significance
rs1287757170	1:175,331,940	G/A	—	pathogenic
rs752447699	1:175,332,894	G/C	—	uncertain significance
rs746082642	1:175,332,924	G/A	—	uncertain significance
rs758987869	1:175,334,166	A/G	—	uncertain significance
rs139865233	1:175,334,183	T/C	—	likely benign
rs767311966	1:175,334,209	C/A	—	uncertain significance
rs767499604	1:175,334,285	C/G	—	uncertain significance
rs371427528	1:175,334,299	C/A	—	uncertain significance
rs2526311223	1:175,334,325	C/G	—	uncertain significance
rs1043341227	1:175,334,362	T/C	—	uncertain significance
rs141636585	1:175,334,409	C/T	—	uncertain significance
rs142291665	1:175,334,630	C/G	—	uncertain significance
rs374910885	1:175,335,098	G/A	—	likely benign
rs949717347	1:175,335,120	C/G	—	uncertain significance
rs202011833	1:175,335,241	G/C	—	uncertain significance
rs199892230	1:175,336,358	A/G	—	uncertain significance
rs147819509	1:175,336,371	C/T	—	uncertain significance
rs73038161	1:175,336,393	G/A	—	likely benign
rs934193155	1:175,336,440	G/T	—	likely benign
rs111763467	1:175,348,712	G/C	—	likely benign
rs137958146	1:175,348,715	C/G	—	uncertain significance
rs859427	1:175,348,723	C/T	missense variant	—
rs779279153	1:175,348,774	A/G	—	uncertain significance
rs776316702	1:175,348,793	C/T	—	uncertain significance
rs139768853	1:175,348,815	G/A	—	likely benign
rs762020704	1:175,348,821	A/G	—	likely benign
rs376736413	1:175,348,837	C/T	—	uncertain significance
rs372205222	1:175,348,850	G/C	—	uncertain significance
rs72723450	1:175,355,152	C/T	—	benign
rs140481433	1:175,355,171	T/C	—	conflicting classifications of pathogenicity
rs149364113	1:175,355,196	G/A	—	benign
rs755698038	1:175,355,210	C/T	—	uncertain significance
rs869312899	1:175,355,213	G/A	—	uncertain significance
rs201193007	1:175,355,216	C/T	—	uncertain significance
rs144742450	1:175,355,217	G/A	—	likely benign
rs748026252	1:175,355,231	C/T	—	uncertain significance
rs776579268	1:175,355,239	C/A	—	uncertain significance
rs2526372402	1:175,355,285	G/C	—	uncertain significance
rs559194241	1:175,355,293	C/A	—	uncertain significance
rs892080402	1:175,355,351	C/T	—	likely pathogenic
rs375626142	1:175,355,352	G/A	—	likely benign
rs138087244	1:175,355,368	G/A	—	uncertain significance
rs859437	1:175,355,391	G/A	—	benign
rs139629961	1:175,355,402	C/T	—	uncertain significance
rs749481817	1:175,355,407	C/A	—	uncertain significance
rs772462129	1:175,355,429	C/A	—	uncertain significance
rs528171911	1:175,360,431	G/A	—	likely benign

Showing 100 of 158 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.