AHCTF1

AT-hook containing transcription factor 1

Summary

Predicted to enable DNA binding activity. Involved in nuclear pore complex assembly and regulation of cytokinesis. Located in chromosome; nuclear body; and nuclear envelope. [provided by Alliance of Genome Resources, Jul 2025]

Known Variants117 total

rsid	Position (GRCh37)	Alleles	Class	ClinVar
rs370639205	1:247,004,125	G/A	—	uncertain significance
rs1659813196	1:247,004,207	T/G	—	uncertain significance
rs1659816925	1:247,004,239	A/C	—	uncertain significance
rs760949626	1:247,004,286	T/C	—	uncertain significance
rs1438700851	1:247,004,290	T/C	—	uncertain significance
rs201853355	1:247,007,165	T/C	—	uncertain significance
rs2527235531	1:247,013,046	C/T	—	uncertain significance
rs527553101	1:247,013,106	G/A	—	uncertain significance
rs776905203	1:247,013,150	T/C	—	uncertain significance
rs779749038	1:247,013,193	A/T	—	uncertain significance
rs772118212	1:247,013,252	T/C	—	uncertain significance
rs201021519	1:247,013,258	C/A	—	uncertain significance
rs763029669	1:247,013,280	T/C	—	uncertain significance
rs752428674	1:247,013,292	T/C	—	uncertain significance
rs1660583568	1:247,013,322	T/G	—	uncertain significance
rs760993765	1:247,013,388	G/A	—	uncertain significance
rs569404964	1:247,013,408	A/G	—	likely benign
rs192835030	1:247,013,424	G/C	—	uncertain significance
rs780228627	1:247,013,481	C/T	—	uncertain significance
rs770884177	1:247,013,507	T/C	—	likely benign
rs376171651	1:247,013,516	C/T	—	uncertain significance
rs142603415	1:247,013,543	T/C	—	likely benign
rs139947110	1:247,013,549	T/G	—	uncertain significance
rs150710000	1:247,013,562	T/G	—	uncertain significance
rs149899496	1:247,013,595	T/C	—	uncertain significance
rs750864401	1:247,013,667	T/C	—	uncertain significance
rs375470134	1:247,013,684	A/G	—	uncertain significance
rs1182388567	1:247,013,691	T/C	—	uncertain significance
rs745619250	1:247,013,703	T/C	—	uncertain significance
rs377251787	1:247,013,753	G/A	—	uncertain significance
rs752758644	1:247,013,823	C/G	—	uncertain significance
rs1438962461	1:247,013,858	T/G	—	uncertain significance
rs138844491	1:247,013,941	G/C	—	uncertain significance
rs1206609542	1:247,014,020	G/C	—	uncertain significance
rs144747230	1:247,014,064	G/A	—	likely benign
rs374602603	1:247,014,075	G/A	—	uncertain significance
rs779757812	1:247,014,230	A/C	—	uncertain significance
rs199542478	1:247,014,241	C/T	—	uncertain significance
rs2527245695	1:247,014,242	A/T	—	uncertain significance
rs576474243	1:247,014,243	T/C	—	likely benign
rs761898045	1:247,014,350	T/C	—	uncertain significance
rs139377503	1:247,014,407	T/C	—	uncertain significance
rs1201409994	1:247,014,693	T/C	—	uncertain significance
rs2527249792	1:247,014,714	C/G	—	uncertain significance
rs200641823	1:247,014,744	C/T	—	uncertain significance
rs143330344	1:247,016,507	C/T	—	likely benign
rs369119391	1:247,016,508	G/A	—	likely benign
rs773513235	1:247,016,542	T/C	—	likely benign
rs750124737	1:247,016,580	T/C	—	uncertain significance
rs779922668	1:247,016,587	G/A	—	uncertain significance
rs2103053909	1:247,019,059	G/A	—	likely benign
rs2527276697	1:247,019,067	G/T	—	uncertain significance
rs757316981	1:247,019,088	T/C	—	uncertain significance
rs754936188	1:247,019,089	C/T	—	uncertain significance
rs760736790	1:247,021,072	C/G	—	uncertain significance
rs780521481	1:247,021,113	T/C	—	uncertain significance
rs2527306470	1:247,024,209	T/A	—	uncertain significance
rs2527307398	1:247,024,293	A/G	—	uncertain significance
rs367758846	1:247,024,345	G/A	—	likely benign
rs774592486	1:247,024,353	G/A	—	uncertain significance
rs561219934	1:247,024,518	C/T	—	likely benign
rs546954676	1:247,024,549	C/T	—	likely benign
rs375978705	1:247,024,564	T/C	—	uncertain significance
rs1558223606	1:247,025,323	G/A	—	uncertain significance
rs139736452	1:247,025,341	G/A	—	uncertain significance
rs753006968	1:247,025,428	T/A	—	uncertain significance
rs915863437	1:247,027,254	T/C	—	uncertain significance
rs776810110	1:247,027,368	T/A	—	uncertain significance
rs562355764	1:247,027,371	G/A	—	likely benign
rs1661776305	1:247,027,389	G/C	—	uncertain significance
rs755035822	1:247,027,418	T/A	—	uncertain significance
rs1482646911	1:247,030,568	T/C	—	uncertain significance
rs753816151	1:247,031,063	T/C	—	uncertain significance
rs531147087	1:247,039,383	C/T	—	uncertain significance
rs369213429	1:247,039,389	A/G	—	uncertain significance
rs778840802	1:247,039,441	T/C	—	uncertain significance
rs369798428	1:247,040,301	T/C	—	uncertain significance
rs200701729	1:247,040,347	C/T	—	uncertain significance
rs61734012	1:247,040,571	T/C	—	likely benign
rs752835319	1:247,040,604	C/T	—	likely benign
rs563410946	1:247,043,342	G/A	—	—
rs535535680	1:247,048,832	C/T	—	uncertain significance
rs565661051	1:247,048,904	T/A	—	uncertain significance
rs2527453036	1:247,048,927	T/C	—	uncertain significance
rs2527461279	1:247,050,527	G/A	—	uncertain significance
rs138324049	1:247,050,575	T/C	—	uncertain significance
rs1663884427	1:247,050,578	C/A	—	uncertain significance
rs778328927	1:247,051,760	C/T	—	uncertain significance
rs745966646	1:247,051,791	T/C	—	uncertain significance
rs183602106	1:247,053,296	G/A	—	uncertain significance
rs763826400	1:247,053,307	T/C	—	uncertain significance
rs201266735	1:247,053,358	T/C	—	uncertain significance
rs141831225	1:247,058,005	G/A	—	uncertain significance
rs769825807	1:247,059,179	G/C	—	uncertain significance
rs1353743980	1:247,059,224	C/T	—	uncertain significance
rs1258343515	1:247,061,569	G/A	—	uncertain significance
rs750243290	1:247,061,574	C/T	—	uncertain significance
rs997749157	1:247,061,632	T/C	—	uncertain significance
rs2527532559	1:247,062,760	T/C	—	uncertain significance
rs1309079601	1:247,063,457	T/C	—	uncertain significance

Showing 100 of 117 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.