TANC1

tetratricopeptide repeat, ankyrin repeat and coiled-coil containing 1

Summary

Predicted to be involved in regulation of postsynapse organization. Predicted to act upstream of or within dendritic spine maintenance; myoblast fusion; and visual learning. Predicted to be located in several cellular components, including axon terminus; neuronal cell body; and postsynaptic density. Predicted to be active in glutamatergic synapse and postsynaptic density, intracellular component. [provided by Alliance of Genome Resources, Jul 2025]

Known Variants127 total

rsid	Position (GRCh37)	Alleles	Class	ClinVar
rs10497203	2:159,851,423	A/C	regulatory region variant	—
rs11674055	2:159,880,105	T/A	—	—
rs264608	2:159,899,188	T/G	—	—
rs7582141	2:159,899,489	G/T	intron variant	—
rs6432512	2:159,899,913	C/T	intron variant	—
rs16843641	2:159,918,378	T/C	intron variant	—
rs2469602920	2:159,922,468	G/A	—	likely benign
rs264651	2:159,929,431	A/G	regulatory region variant	—
rs264588	2:159,936,391	C/T	—	—
rs56277867	2:159,948,474	A/T	—	—
rs264631	2:159,950,865	C/G	regulatory region variant	—
rs34588551	2:159,954,175	C/T	missense variant	—
rs2046279146	2:159,954,241	T/C	—	uncertain significance
rs114704202	2:159,954,295	C/A	—	benign
rs55654562	2:159,958,894	C/T	intron variant	—
rs34324915	2:159,983,207	A/T	regulatory region variant	—
rs73969456	2:159,983,331	C/T	regulatory region variant	—
rs891906625	2:160,005,674	C/T	—	uncertain significance
rs748774322	2:160,005,683	C/T	—	uncertain significance
rs200122820	2:160,005,743	G/C	—	uncertain significance
rs193207814	2:160,005,762	T/C	—	likely benign
rs1340714935	2:160,006,948	C/A	—	uncertain significance
rs759065591	2:160,006,991	G/A	—	likely benign
rs757660211	2:160,007,065	T/C	—	uncertain significance
rs547073714	2:160,007,260	T/C	—	—
rs183131700	2:160,014,055	G/A	regulatory region variant	—
rs55929944	2:160,019,901	C/T	—	benign
rs373966014	2:160,019,961	A/G	—	uncertain significance
rs761085123	2:160,025,767	G/A	—	uncertain significance
rs1376401970	2:160,025,784	G/T	—	uncertain significance
rs545025376	2:160,025,801	C/T	—	likely benign
rs754760244	2:160,025,824	G/A	—	uncertain significance
rs371346675	2:160,025,827	C/T	—	uncertain significance
rs777417010	2:160,025,832	A/G	—	uncertain significance
rs764220742	2:160,025,875	A/T	—	uncertain significance
rs767476734	2:160,027,044	C/T	—	uncertain significance
rs747407663	2:160,027,149	T/A	—	uncertain significance
rs371199083	2:160,027,272	G/T	—	uncertain significance
rs1310670940	2:160,027,275	T/A	—	uncertain significance
rs776468613	2:160,027,299	C/T	—	uncertain significance
rs191513433	2:160,027,304	T/G	—	uncertain significance
rs762586930	2:160,028,638	A/T	—	uncertain significance
rs2055328036	2:160,028,661	A/G	—	uncertain significance
rs2469086245	2:160,028,715	C/T	—	uncertain significance
rs377158840	2:160,028,716	C/G	—	uncertain significance
rs143763614	2:160,028,733	G/A	—	uncertain significance
rs768526084	2:160,035,076	A/C	—	uncertain significance
rs771019464	2:160,035,113	T/C	—	uncertain significance
rs2469205135	2:160,035,129	C/A	—	uncertain significance
rs755192711	2:160,035,200	C/T	—	uncertain significance
rs769934745	2:160,035,208	G/A	—	uncertain significance
rs200461468	2:160,035,260	G/A	—	uncertain significance
rs936415017	2:160,035,275	A/G	—	uncertain significance
rs759947128	2:160,035,379	C/G	—	uncertain significance
rs768556651	2:160,035,422	G/A	—	uncertain significance
rs375321124	2:160,035,442	G/A	—	uncertain significance
rs2056168561	2:160,035,483	C/G	—	uncertain significance
rs534711706	2:160,035,608	C/T	—	uncertain significance
rs987527475	2:160,043,437	T/G	—	uncertain significance
rs111308152	2:160,043,467	G/A	—	uncertain significance
rs774260498	2:160,043,491	G/A	—	uncertain significance
rs2469368495	2:160,043,506	C/G	—	uncertain significance
rs374465130	2:160,043,530	G/A	—	uncertain significance
rs778915555	2:160,050,775	G/A	—	uncertain significance
rs374498239	2:160,050,855	C/T	—	uncertain significance
rs768415905	2:160,050,880	C/G	—	uncertain significance
rs1310313241	2:160,050,927	G/A	—	uncertain significance
rs768772022	2:160,053,126	A/G	—	uncertain significance
rs777299338	2:160,053,170	C/T	—	uncertain significance
rs753526166	2:160,053,171	G/A	—	uncertain significance
rs749499631	2:160,055,491	C/T	—	likely benign
rs745896730	2:160,055,510	G/A	—	uncertain significance
rs372204559	2:160,055,519	C/A	—	uncertain significance
rs13022357	2:160,069,756	A/G	intron variant	—
rs372287259	2:160,074,022	G/A	—	uncertain significance
rs1435380586	2:160,074,116	G/A	—	uncertain significance
rs182262741	2:160,075,772	C/T	—	likely benign
rs375860483	2:160,075,851	G/C	—	uncertain significance
rs758237953	2:160,075,857	T/C	—	uncertain significance
rs779632178	2:160,076,304	G/A	—	uncertain significance
rs768936831	2:160,076,334	C/T	—	uncertain significance
rs372839518	2:160,076,367	G/A	—	uncertain significance
rs202039152	2:160,076,373	G/A	—	uncertain significance
rs753021908	2:160,080,743	G/A	—	uncertain significance
rs746901684	2:160,080,770	G/A	—	uncertain significance
rs377392032	2:160,080,780	A/G	—	uncertain significance
rs201866379	2:160,080,820	C/A	—	likely benign
rs908691835	2:160,082,204	G/A	—	uncertain significance
rs749043695	2:160,082,266	G/T	—	uncertain significance
rs371866385	2:160,082,288	A/G	—	uncertain significance
rs371240519	2:160,085,371	C/G	—	uncertain significance
rs369527846	2:160,086,095	C/G	—	uncertain significance
rs539614156	2:160,086,096	G/A	—	uncertain significance
rs1218214958	2:160,086,129	A/C	—	uncertain significance
rs200295160	2:160,086,255	G/A	—	uncertain significance
rs2060241475	2:160,086,338	G/T	—	uncertain significance
rs750477249	2:160,086,403	G/A	—	uncertain significance
rs777340260	2:160,086,424	A/G	—	uncertain significance
rs371803281	2:160,086,441	G/C	—	uncertain significance
rs761006466	2:160,086,446	G/A	—	likely benign

Showing 100 of 127 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.