ZNF462

zinc finger protein 462

Summary

The protein encoded by this gene belongs to C2H2-type zinc finger family of proteins. It contains multiple C2H2-type zinc fingers and may be involved in transcriptional regulation. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Dec 2016]

Known Variants363 total

rsid	Position (GRCh37)	Alleles	Class	ClinVar
rs35277765	9:109,622,801	G/T	—	benign
rs1403803276	9:109,626,280	G/C	—	uncertain significance
rs4743033	9:109,627,913	A/C	—	—
rs73667301	9:109,628,051	A/G	intron variant	—
rs4743034	9:109,632,353	G/A	intron variant	—
rs551038039	9:109,636,133	T/C	—	—
rs4743038	9:109,645,987	A/T	intron variant	—
rs935747402	9:109,651,662	T/C	—	—
rs1858231	9:109,676,893	A/G	intron variant	—
rs146521601	9:109,685,706	G/A	—	likely benign
rs750966412	9:109,685,748	G/A	—	likely benign
rs747677472	9:109,685,782	A/G	—	likely benign
rs1830066702	9:109,685,786	T/C	—	uncertain significance
rs745655320	9:109,685,808	C/T	—	likely benign
rs199632466	9:109,685,809	G/A	—	likely benign
rs2538698643	9:109,685,837	A/C	—	uncertain significance
rs2538698752	9:109,685,842	T/C	—	uncertain significance
rs763391765	9:109,685,845	T/A	—	uncertain significance
rs1830071684	9:109,685,883	A/G	—	uncertain significance
rs2131431481	9:109,685,885	G/A	—	pathogenic
rs2538710070	9:109,686,423	C/A	—	uncertain significance
rs149559819	9:109,686,430	A/T	—	likely benign
rs41277819	9:109,686,431	T/C	—	likely benign
rs770953097	9:109,686,457	C/A	—	uncertain significance
rs759913484	9:109,686,465	G/C	—	uncertain significance
rs1454295232	9:109,686,506	A/G	—	uncertain significance
rs2538713678	9:109,686,581	G/C	—	uncertain significance
rs200191214	9:109,686,603	G/A	—	likely benign
rs777936918	9:109,686,607	T/A	—	uncertain significance
rs140067056	9:109,686,634	C/A	—	likely benign
rs751537020	9:109,686,658	C/T	—	likely benign
rs779724967	9:109,686,659	G/A	—	uncertain significance
rs1418374583	9:109,686,700	C/A	—	pathogenic
rs2538716463	9:109,686,704	T/G	—	uncertain significance
rs142022589	9:109,686,770	A/G	—	likely benign
rs370249991	9:109,686,780	C/A	—	uncertain significance
rs767449244	9:109,686,797	A/G	—	uncertain significance
rs199521620	9:109,686,816	C/T	—	likely benign
rs139468672	9:109,686,820	C/T	—	likely benign
rs755534398	9:109,686,821	G/A	—	uncertain significance
rs149654492	9:109,686,826	A/G	—	likely benign
rs762473377	9:109,686,828	T/C	—	uncertain significance
rs561253375	9:109,686,855	C/T	—	likely benign
rs2538720827	9:109,686,911	C/T	—	pathogenic
rs2538720975	9:109,686,922	T/C	—	likely benign
rs1588062809	9:109,686,956	C/T	—	pathogenic
rs2131446280	9:109,686,998	A/G	—	uncertain significance
rs778521296	9:109,687,031	C/A	—	conflicting classifications of pathogenicity
rs2538722843	9:109,687,038	G/A	—	uncertain significance
rs767585171	9:109,687,054	T/C	—	likely benign
rs752732489	9:109,687,056	T/G	—	uncertain significance
rs1830123851	9:109,687,082	A/C	—	uncertain significance
rs1830123953	9:109,687,083	C/G	—	uncertain significance
rs767635208	9:109,687,120	C/G	—	likely benign
rs200116056	9:109,687,121	C/G	—	uncertain significance
rs139165480	9:109,687,139	A/G	—	uncertain significance
rs1830128291	9:109,687,175	A/G	—	uncertain significance
rs772326829	9:109,687,209	C/T	—	uncertain significance
rs2538727019	9:109,687,245	C/G	—	uncertain significance
rs73522973	9:109,687,257	G/A	—	likely benign
rs756115437	9:109,687,261	A/G	—	likely benign
rs140936337	9:109,687,269	T/G	—	likely benign
rs1000152	9:109,687,288	T/C	—	benign
rs773629680	9:109,687,308	A/T	—	uncertain significance
rs747318702	9:109,687,319	G/A	—	uncertain significance
rs1830136626	9:109,687,366	G/C	—	uncertain significance
rs941195715	9:109,687,371	A/G	—	uncertain significance
rs17723637	9:109,687,403	A/G	missense variant	benign
rs2538731823	9:109,687,491	G/C	—	uncertain significance
rs2538732133	9:109,687,512	A/T	—	uncertain significance
rs2131454461	9:109,687,544	C/T	—	likely pathogenic
rs2538733841	9:109,687,637	T/C	—	uncertain significance
rs73522975	9:109,687,639	G/A	—	benign
rs1830147574	9:109,687,653	C/T	—	uncertain significance
rs756323605	9:109,687,679	A/G	—	uncertain significance
rs2538735078	9:109,687,712	G/A	—	uncertain significance
rs144070292	9:109,687,752	A/T	—	uncertain significance
rs779079488	9:109,687,773	G/A	—	likely benign
rs780767515	9:109,687,801	C/T	—	likely benign
rs200349681	9:109,687,821	C/T	—	benign
rs146183570	9:109,687,834	A/G	—	benign
rs2131459000	9:109,687,835	C/T	—	uncertain significance
rs368056745	9:109,687,836	C/T	—	likely benign
rs199560820	9:109,687,837	G/A	—	likely benign
rs145644535	9:109,687,839	C/T	—	likely benign
rs201035963	9:109,687,840	G/A	—	likely benign
rs200388230	9:109,687,841	C/T	—	likely benign
rs750520083	9:109,687,843	G/A	—	likely benign
rs1379106674	9:109,687,883	C/T	—	pathogenic
rs2538739733	9:109,687,902	C/T	—	uncertain significance
rs2538740342	9:109,687,928	C/A	—	uncertain significance
rs745760296	9:109,687,947	C/T	—	likely benign
rs2538740857	9:109,687,950	A/T	—	uncertain significance
rs763301819	9:109,687,975	C/T	—	likely benign
rs201536868	9:109,687,976	G/A	—	likely benign
rs534168298	9:109,688,027	C/G	—	uncertain significance
rs2131463464	9:109,688,111	C/T	—	uncertain significance
rs1045510089	9:109,688,139	C/T	—	likely benign
rs1830173812	9:109,688,145	C/T	—	uncertain significance
rs2131464445	9:109,688,169	A/T	—	uncertain significance

Showing 100 of 363 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.