TNNI3K

TNNI3 interacting kinase

Summary

This gene encodes a protein that belongs to the MAP kinase kinase kinase (MAPKKK) family of protein kinases. The protein contains ankyrin repeat, protein kinase and serine-rich domains and is thought to play a role in cardiac physiology. [provided by RefSeq, Sep 2012]

Known Variants824 total

rsid	Position (GRCh37)	Alleles	Class	ClinVar
rs2524303900	1:74,701,136	A/G	—	uncertain significance
rs2524303907	1:74,701,137	T/A	—	uncertain significance
rs2524304033	1:74,701,154	A/G	—	uncertain significance
rs370113173	1:74,701,156	A/G	—	likely benign
rs750523606	1:74,701,157	C/T	—	uncertain significance
rs756332135	1:74,701,158	C/A	—	uncertain significance
rs2524304081	1:74,701,162	C/A	—	likely benign
rs2524304094	1:74,701,163	C/A	—	uncertain significance
rs200469447	1:74,701,170	G/A	—	uncertain significance
rs1451279328	1:74,701,172	A/G	—	uncertain significance
rs2100818863	1:74,701,177	T/C	—	uncertain significance
rs505508	1:74,701,295	T/A	—	benign
rs500203	1:74,701,651	A/T	—	benign
rs1053164979	1:74,701,767	A/G	—	likely benign
rs756240367	1:74,701,771	G/C	—	likely benign
rs780321887	1:74,701,774	C/T	—	likely benign
rs2524307164	1:74,701,786	A/G	—	uncertain significance
rs144055969	1:74,701,787	T/A	—	uncertain significance
rs2524307176	1:74,701,788	G/A	—	uncertain significance
rs2524307211	1:74,701,802	A/T	—	uncertain significance
rs1653844095	1:74,701,821	A/G	—	uncertain significance
rs1653844435	1:74,701,822	T/C	—	uncertain significance
rs2524307409	1:74,701,826	A/G	—	likely benign
rs2524307444	1:74,701,830	G/A	—	uncertain significance
rs1406241089	1:74,701,834	G/T	—	uncertain significance
rs904118557	1:74,701,835	A/G	—	likely benign
rs1397678696	1:74,701,837	T/G	—	uncertain significance
rs147478946	1:74,701,851	C/T	—	uncertain significance
rs774789454	1:74,701,866	G/T	—	uncertain significance
rs1653847391	1:74,701,872	A/G	—	uncertain significance
rs767822797	1:74,701,886	T/C	—	benign
rs1653847996	1:74,701,887	A/G	—	uncertain significance
rs761013097	1:74,701,899	A/T	—	uncertain significance
rs200192647	1:74,701,903	G/A	—	likely benign
rs2524307909	1:74,701,907	G/C	—	uncertain significance
rs2524307949	1:74,701,911	C/A	—	uncertain significance
rs1653850183	1:74,701,912	A/C	—	likely benign
rs532221	1:74,701,950	T/A	—	benign
rs1449603518	1:74,715,134	T/A	—	likely benign
rs2100845206	1:74,715,138	T/C	—	likely benign
rs750231167	1:74,715,139	T/C	—	likely benign
rs1480436537	1:74,715,140	C/T	—	uncertain significance
rs1165242749	1:74,715,149	T/A	—	uncertain significance
rs779669223	1:74,715,157	T/G	—	uncertain significance
rs748943581	1:74,715,158	C/A	—	uncertain significance
rs201179498	1:74,715,159	A/T	—	uncertain significance
rs2524364025	1:74,715,164	A/T	—	uncertain significance
rs2524364035	1:74,715,165	G/C	—	uncertain significance
rs780477698	1:74,715,168	A/G	—	uncertain significance
rs199714304	1:74,715,169	A/G	—	conflicting classifications of pathogenicity
rs749773017	1:74,715,175	A/G	—	uncertain significance
rs2100845317	1:74,715,179	C/A	—	uncertain significance
rs567503494	1:74,715,181	G/A	—	uncertain significance
rs2524364159	1:74,715,182	C/T	—	likely benign
rs371211761	1:74,715,185	T/C	—	likely benign
rs201061482	1:74,715,186	G/T	—	conflicting classifications of pathogenicity
rs374710618	1:74,715,188	A/T	—	uncertain significance
rs747376388	1:74,715,193	G/A	—	uncertain significance
rs2100845353	1:74,715,194	G/A	—	likely benign
rs2524364263	1:74,715,197	G/T	—	likely benign
rs1246062657	1:74,715,198	T/A	—	uncertain significance
rs140940650	1:74,715,204	C/T	—	uncertain significance
rs1654797621	1:74,715,217	G/T	—	uncertain significance
rs1388062726	1:74,715,228	G/A	—	uncertain significance
rs1654798958	1:74,715,229	G/A	—	uncertain significance
rs767445454	1:74,715,231	G/A	—	uncertain significance
rs750425525	1:74,715,233	G/A	—	uncertain significance
rs2524364652	1:74,715,240	A/C	—	likely benign
rs2100845521	1:74,715,248	T/C	—	likely benign
rs45487595	1:74,716,310	C/A	—	benign
rs201012396	1:74,716,338	T/C	—	likely benign
rs1310393809	1:74,716,347	C/T	—	likely benign
rs760637494	1:74,716,353	A/G	—	uncertain significance
rs766113814	1:74,716,354	A/G	—	uncertain significance
rs201209296	1:74,716,365	C/G	—	uncertain significance
rs2100847673	1:74,716,368	A/G	—	uncertain significance
rs202213063	1:74,716,369	T/C	—	likely benign
rs757956610	1:74,716,370	A/G	—	uncertain significance
rs752068095	1:74,716,373	C/T	—	uncertain significance
rs200318618	1:74,716,374	G/A	—	uncertain significance
rs201074684	1:74,716,383	T/A	—	uncertain significance
rs780125125	1:74,716,397	C/T	—	uncertain significance
rs749552940	1:74,716,398	G/A	—	uncertain significance
rs1343968991	1:74,716,399	C/T	—	likely benign
rs774437316	1:74,716,407	G/A	—	uncertain significance
rs1452380676	1:74,716,409	C/G	—	uncertain significance
rs746891147	1:74,716,410	T/G	—	uncertain significance
rs192894824	1:74,716,413	C/A	—	likely benign
rs183819545	1:74,716,420	T/C	—	likely benign
rs1570370552	1:74,716,431	C/G	—	uncertain significance
rs1654879777	1:74,716,432	C/A	—	likely benign
rs1205906347	1:74,716,435	G/A	—	likely benign
rs142238660	1:74,716,436	C/G	—	uncertain significance
rs2524369636	1:74,716,438	T/A	—	uncertain significance
rs140333244	1:74,716,443	C/T	—	likely benign
rs774973228	1:74,716,445	G/A	—	uncertain significance
rs1007039876	1:74,716,450	C/G	—	uncertain significance
rs2524369715	1:74,716,454	G/A	—	uncertain significance
rs762721434	1:74,716,455	T/C	—	uncertain significance
rs2100847853	1:74,716,456	A/C	—	uncertain significance

Showing 100 of 824 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.