STAG1

STAG1 cohesin complex component

Summary

This gene is a member of the SCC3 family and is expressed in the nucleus. It encodes a component of cohesin, a multisubunit protein complex that provides sister chromatid cohesion along the length of a chromosome from DNA replication through prophase and prometaphase, after which it is dissociated in preparation for segregation during anaphase. [provided by RefSeq, Jul 2008]

Known Variants400 total

rsid	Position (GRCh37)	Alleles	Class	ClinVar
rs1935782463	3:136,057,112	C/G	—	uncertain significance
rs1483651821	3:136,057,200	T/C	—	likely benign
rs376501222	3:136,057,204	A/C	—	uncertain significance
rs1194869720	3:136,057,205	C/T	—	likely benign
rs757098419	3:136,057,214	A/T	—	uncertain significance
rs192497288	3:136,057,239	G/A	—	likely benign
rs1935793739	3:136,057,273	C/T	—	uncertain significance
rs2530008022	3:136,057,274	G/A	—	likely pathogenic
rs374980869	3:136,059,317	T/C	—	likely benign
rs778261236	3:136,059,335	G/A	—	likely benign
rs372781554	3:136,059,370	A/G	—	uncertain significance
rs2530017867	3:136,059,424	G/A	—	uncertain significance
rs1022520130	3:136,059,441	A/G	—	likely benign
rs1314421660	3:136,059,442	C/T	—	uncertain significance
rs1935927985	3:136,059,446	G/A	—	likely pathogenic
rs3821444	3:136,059,461	G/A	—	benign
rs757663777	3:136,060,294	C/T	—	likely benign
rs1210184509	3:136,060,296	C/T	—	uncertain significance
rs1026553102	3:136,060,304	C/T	—	conflicting classifications of pathogenicity
rs1424000086	3:136,060,314	T/C	—	uncertain significance
rs1042814423	3:136,060,323	T/G	—	uncertain significance
rs951011605	3:136,060,334	T/C	—	uncertain significance
rs747617236	3:136,060,340	C/T	—	uncertain significance
rs2530021558	3:136,060,341	G/C	—	uncertain significance
rs201648959	3:136,060,351	T/C	—	likely benign
rs2530021619	3:136,060,352	T/C	—	likely pathogenic
rs1192501955	3:136,060,357	C/T	—	likely benign
rs926941672	3:136,060,360	C/T	—	likely benign
rs1300433502	3:136,060,361	G/A	—	uncertain significance
rs937043439	3:136,060,378	G/A	—	likely benign
rs376238432	3:136,062,655	A/G	—	likely benign
rs1936101809	3:136,062,660	T/A	—	likely benign
rs2530031168	3:136,062,673	C/T	—	likely pathogenic
rs2530031200	3:136,062,676	G/T	—	likely benign
rs747646536	3:136,062,685	G/A	—	likely benign
rs1936103411	3:136,062,698	C/A	—	uncertain significance
rs368883876	3:136,062,708	A/T	—	likely benign
rs1381188958	3:136,062,719	T/G	—	uncertain significance
rs34149860	3:136,062,724	C/G	missense variant	benign
rs759432131	3:136,062,735	T/C	—	uncertain significance
rs775333952	3:136,062,736	G/A	—	likely benign
rs760773777	3:136,062,740	C/T	—	likely benign
rs776820207	3:136,062,752	C/T	—	conflicting classifications of pathogenicity
rs1032980741	3:136,062,753	G/A	—	uncertain significance
rs761963794	3:136,062,756	G/A	—	likely benign
rs758713527	3:136,062,769	G/A	—	likely benign
rs752047790	3:136,062,778	T/C	—	likely benign
rs755648970	3:136,062,779	G/A	—	likely benign
rs543312959	3:136,062,781	T/C	—	benign
rs1936109432	3:136,062,786	G/C	—	uncertain significance
rs1936109702	3:136,062,788	G/A	—	uncertain significance
rs1398765954	3:136,062,790	G/A	—	likely benign
rs2530032072	3:136,062,795	G/A	—	uncertain significance
rs997104717	3:136,062,807	T/C	—	uncertain significance
rs748823468	3:136,062,808	G/T	—	likely benign
rs756906447	3:136,062,816	T/A	—	likely benign
rs1326581908	3:136,062,828	A/G	—	uncertain significance
rs1936112483	3:136,062,831	T/G	—	uncertain significance
rs372448385	3:136,062,844	C/G	—	uncertain significance
rs375738588	3:136,067,982	G/C	—	benign
rs2530050552	3:136,067,995	C/T	—	uncertain significance
rs1267304310	3:136,068,030	G/A	—	likely pathogenic
rs143545882	3:136,068,055	G/A	—	likely benign
rs1377634957	3:136,068,056	G/T	—	uncertain significance
rs748207104	3:136,068,079	G/A	—	likely benign
rs2108267944	3:136,068,087	A/G	—	uncertain significance
rs1362041873	3:136,068,112	G/A	—	likely benign
rs199902670	3:136,068,167	A/G	—	conflicting classifications of pathogenicity
rs1239483845	3:136,068,170	A/G	—	uncertain significance
rs150499884	3:136,068,178	G/A	—	likely benign
rs2530051248	3:136,068,203	T/A	—	uncertain significance
rs1268657053	3:136,068,209	G/T	—	conflicting classifications of pathogenicity
rs371335681	3:136,068,218	T/C	—	likely benign
rs1457682068	3:136,076,542	T/C	—	likely benign
rs1229784300	3:136,076,552	T/C	—	likely benign
rs2530078152	3:136,076,581	G/A	—	pathogenic
rs761204996	3:136,076,594	A/T	—	likely benign
rs2530078235	3:136,076,624	C/T	—	likely benign
rs1560055490	3:136,076,656	G/C	—	uncertain significance
rs367902665	3:136,076,702	G/T	—	likely benign
rs2530078524	3:136,076,707	T/C	—	likely benign
rs1471479119	3:136,077,990	T/C	—	conflicting classifications of pathogenicity
rs1006344504	3:136,078,002	G/C	—	likely benign
rs755929141	3:136,078,037	A/G	—	likely benign
rs61748114	3:136,078,040	T/C	—	benign
rs2530083693	3:136,078,096	T/C	—	uncertain significance
rs200155287	3:136,078,108	G/T	—	uncertain significance
rs745946457	3:136,078,110	C/A	—	uncertain significance
rs1052219141	3:136,078,141	G/A	—	uncertain significance
rs1327541204	3:136,078,154	A/G	—	likely benign
rs2530084194	3:136,078,156	A/G	—	likely benign
rs2108286877	3:136,082,242	T/C	—	uncertain significance
rs150048785	3:136,082,253	A/C	—	likely benign
rs367692062	3:136,082,254	A/G	—	uncertain significance
rs2530103284	3:136,082,271	C/G	—	likely benign
rs201431655	3:136,082,321	A/G	—	likely benign
rs533285816	3:136,082,324	A/G	—	likely benign
rs771633152	3:136,085,766	T/C	—	likely benign
rs1251552724	3:136,085,787	T/C	—	uncertain significance
rs1259971597	3:136,085,797	T/C	—	likely benign

Showing 100 of 400 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.