YY1AP1

YY1 associated protein 1

Summary

Involved in cell differentiation; cell population proliferation; and regulation of cell cycle. Located in Ino80 complex; fibrillar center; and nucleoplasm. [provided by Alliance of Genome Resources, Jul 2025]

Known Variants102 total

rsid	Position (GRCh37)	Alleles	Class	ClinVar
rs143518160	1:155,629,451	A/G	—	benign
rs556811436	1:155,629,522	A/T	—	uncertain significance
rs201827011	1:155,629,600	T/C	—	uncertain significance
rs1371665336	1:155,629,606	G/A	—	uncertain significance
rs199876978	1:155,629,614	C/T	—	uncertain significance
rs1352962597	1:155,629,628	T/C	—	likely benign
rs202044617	1:155,629,648	C/T	—	uncertain significance
rs1057519598	1:155,629,714	C/A	stop gained	pathogenic
rs1057519597	1:155,629,725	A/T	stop gained	pathogenic
rs1259423828	1:155,629,752	T/C	—	uncertain significance
rs146837303	1:155,629,762	C/T	—	likely benign
rs537349	1:155,629,792	T/C	—	likely benign
rs371356803	1:155,629,878	A/G	—	uncertain significance
rs397834368	1:155,629,928	G/A	—	likely benign
rs1414638464	1:155,629,939	T/C	—	uncertain significance
rs145401844	1:155,629,946	G/A	—	likely benign
rs76776727	1:155,629,964	C/T	—	benign
rs376401461	1:155,629,968	T/C	—	likely benign
rs145852062	1:155,629,982	C/T	—	benign
rs2525585024	1:155,629,993	C/T	—	uncertain significance
rs150387705	1:155,630,058	A/G	—	uncertain significance
rs752169560	1:155,630,119	G/A	—	uncertain significance
rs1478753085	1:155,630,173	T/C	—	uncertain significance
rs372660268	1:155,630,217	G/A	—	uncertain significance
rs142902174	1:155,630,240	G/A	—	likely benign
rs373553503	1:155,630,241	G/C	—	uncertain significance
rs185936522	1:155,630,245	T/C	—	benign
rs2525589694	1:155,630,275	T/G	—	uncertain significance
rs775904959	1:155,630,284	C/T	—	uncertain significance
rs144795941	1:155,630,296	G/C	—	benign
rs777752993	1:155,630,352	A/G	—	uncertain significance
rs145508654	1:155,630,362	C/T	—	uncertain significance
rs113197997	1:155,630,397	T/C	—	benign
rs1189727690	1:155,630,432	G/A	—	likely benign
rs138828274	1:155,630,499	T/C	—	likely benign
rs201580131	1:155,630,509	G/A	—	uncertain significance
rs141378369	1:155,630,543	C/T	—	benign
rs149619998	1:155,630,552	T/C	—	likely benign
rs748756201	1:155,630,565	C/T	—	uncertain significance
rs531261237	1:155,630,566	G/A	—	uncertain significance
rs2525594745	1:155,630,640	T/C	—	uncertain significance
rs150614243	1:155,630,673	C/T	—	likely benign
rs1187632357	1:155,631,108	A/G	—	uncertain significance
rs765633658	1:155,631,118	G/A	—	uncertain significance
rs56737889	1:155,631,119	G/A	—	likely benign
rs372439408	1:155,631,171	C/G	—	uncertain significance
rs549885951	1:155,631,201	G/T	—	uncertain significance
rs545822524	1:155,638,425	A/G	—	uncertain significance
rs371056637	1:155,638,475	T/G	—	uncertain significance
rs151172022	1:155,638,479	C/T	—	likely benign
rs1649426507	1:155,638,524	A/C	—	uncertain significance
rs761538372	1:155,638,568	A/C	—	uncertain significance
rs1181610432	1:155,640,137	C/T	—	likely benign
rs773985151	1:155,640,243	G/T	—	uncertain significance
rs1558307853	1:155,642,328	A/C	—	pathogenic
rs1366840083	1:155,642,359	T/C	—	uncertain significance
rs773128473	1:155,642,367	T/A	—	uncertain significance
rs144227023	1:155,642,477	G/C	—	uncertain significance
rs759807181	1:155,642,492	T/C	—	uncertain significance
rs1395132982	1:155,642,501	G/C	—	uncertain significance
rs199653824	1:155,642,523	C/T	—	pathogenic
rs374748241	1:155,644,807	T/C	—	uncertain significance
rs1278358196	1:155,644,809	T/C	—	uncertain significance
rs367625562	1:155,644,828	C/T	—	likely benign
rs201603249	1:155,646,332	G/A	—	likely benign
rs749232831	1:155,646,353	G/A	stop gained	pathogenic
rs2525775532	1:155,646,403	T/G	—	uncertain significance
rs1057519599	1:155,646,413	G/A	stop gained	pathogenic
rs375078184	1:155,646,438	C/G	—	uncertain significance
rs1026131024	1:155,646,490	G/A	—	likely benign
rs762972281	1:155,649,267	C/G	—	uncertain significance
rs775549264	1:155,649,278	T/C	—	uncertain significance
rs138164527	1:155,649,287	C/A	—	uncertain significance
rs572787452	1:155,651,116	C/T	—	—
rs778646700	1:155,657,861	C/A	—	likely pathogenic
rs1466553299	1:155,657,868	G/A	—	likely pathogenic
rs149449921	1:155,657,871	G/A	—	benign
rs76443098	1:155,657,890	A/G	—	benign
rs143953255	1:155,657,901	A/G	—	likely benign
rs139279518	1:155,657,931	G/A	—	uncertain significance
rs61817761	1:155,657,936	C/T	—	benign
rs188043733	1:155,657,982	G/A	—	uncertain significance
rs1017809059	1:155,657,986	A/T	—	likely benign
rs535995489	1:155,658,012	G/A	—	uncertain significance
rs72999042	1:155,658,015	G/A	—	conflicting classifications of pathogenicity
rs1180832151	1:155,658,026	T/C	—	likely benign
rs533867635	1:155,658,030	G/A	—	uncertain significance
rs758007166	1:155,658,035	A/T	—	pathogenic
rs751314743	1:155,658,050	G/A	—	uncertain significance
rs1558323022	1:155,658,053	G/A	—	uncertain significance
rs114089731	1:155,658,060	A/G	—	likely benign
rs927165270	1:155,658,076	T/C	—	likely benign
rs1235940092	1:155,658,081	T/C	—	uncertain significance
rs769324996	1:155,658,083	G/T	—	uncertain significance
rs201953751	1:155,658,114	G/A	—	uncertain significance
rs111718014	1:155,658,118	G/A	—	likely benign
rs1039294641	1:155,658,153	C/G	—	uncertain significance
rs748677612	1:155,658,177	C/T	—	uncertain significance
rs1399334270	1:155,658,178	T/C	—	likely benign
rs2525946529	1:155,658,198	C/T	—	uncertain significance

Showing 100 of 102 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.