ZNF142

zinc finger protein 142

Summary

The protein encoded by this gene belongs to the Kruppel family of C2H2-type zinc finger proteins. It contains 31 C2H2-type zinc fingers and may be involved in transcriptional regulation. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Jan 2013]

Known Variants208 total

rsid	Position (GRCh37)	Alleles	Class	ClinVar
rs2384950	2:219,499,719	T/A	—	—
rs193157475	2:219,503,088	C/T	—	likely benign
rs1803383	2:219,503,113	C/T	—	benign
rs2469615557	2:219,503,132	A/G	—	uncertain significance
rs1216015544	2:219,503,208	C/T	—	conflicting classifications of pathogenicity
rs556339609	2:219,503,278	G/A	—	likely benign
rs1696902295	2:219,503,279	G/A	—	uncertain significance
rs370013089	2:219,503,318	C/A	—	uncertain significance
rs200894546	2:219,503,327	C/T	—	uncertain significance
rs373369883	2:219,503,328	G/A	—	likely benign
rs200133906	2:219,503,348	T/A	—	uncertain significance
rs183954984	2:219,503,358	C/T	—	uncertain significance
rs372969531	2:219,503,396	C/T	—	uncertain significance
rs200757676	2:219,503,420	T/C	—	uncertain significance
rs770886397	2:219,503,435	G/C	—	uncertain significance
rs1383766082	2:219,503,438	C/T	—	uncertain significance
rs756225038	2:219,503,472	G/A	—	conflicting classifications of pathogenicity
rs780339522	2:219,503,486	C/T	—	uncertain significance
rs746988011	2:219,503,508	C/T	—	uncertain significance
rs2469638641	2:219,505,386	C/G	—	likely pathogenic
rs72962069	2:219,505,465	G/A	—	likely benign
rs367658234	2:219,505,483	G/A	—	likely pathogenic
rs756892380	2:219,506,877	G/A	—	likely benign
rs540993510	2:219,506,890	C/T	—	uncertain significance
rs775858349	2:219,506,896	C/G	—	uncertain significance
rs772191289	2:219,506,935	T/C	—	uncertain significance
rs773306836	2:219,506,938	C/T	—	uncertain significance
rs759433449	2:219,506,939	G/A	—	uncertain significance
rs866857892	2:219,506,959	G/A	—	uncertain significance
rs751295416	2:219,506,960	G/A	—	uncertain significance
rs899592686	2:219,507,011	C/T	—	uncertain significance
rs1265214128	2:219,507,047	G/A	—	uncertain significance
rs748323893	2:219,507,054	C/T	—	no classification for the single variant
rs1272050636	2:219,507,064	C/T	—	uncertain significance
rs778031136	2:219,507,122	G/A	—	uncertain significance
rs775478121	2:219,507,142	C/T	—	uncertain significance
rs200075933	2:219,507,148	G/C	—	uncertain significance
rs114603798	2:219,507,166	G/A	—	likely benign
rs374554076	2:219,507,208	C/T	—	uncertain significance
rs201080085	2:219,507,217	G/A	—	uncertain significance
rs766056018	2:219,507,241	C/A	—	uncertain significance
rs759147770	2:219,507,245	G/A	—	uncertain significance
rs1338342481	2:219,507,268	G/A	—	uncertain significance
rs3821033	2:219,507,302	C/T	—	benign
rs776415431	2:219,507,317	G/A	—	likely pathogenic
rs200895363	2:219,507,352	C/G	—	uncertain significance
rs780238469	2:219,507,368	A/G	—	uncertain significance
rs746779277	2:219,507,386	C/G	—	uncertain significance
rs774915135	2:219,507,433	C/T	—	uncertain significance
rs1441083699	2:219,507,439	T/A	—	uncertain significance
rs755179850	2:219,507,452	C/T	—	uncertain significance
rs200823502	2:219,507,460	G/A	—	uncertain significance
rs1575061502	2:219,507,485	C/T	—	uncertain significance
rs2469664653	2:219,507,505	A/T	—	pathogenic
rs200398690	2:219,507,508	C/T	—	uncertain significance
rs140912415	2:219,507,531	C/T	—	likely benign
rs1275959058	2:219,507,541	C/A	—	likely pathogenic
rs1304332178	2:219,507,599	G/A	—	uncertain significance
rs374587127	2:219,507,604	C/T	—	uncertain significance
rs376888579	2:219,507,622	T/C	—	uncertain significance
rs1170965803	2:219,507,648	C/T	—	likely benign
rs61733613	2:219,507,666	C/T	—	benign
rs759312228	2:219,507,682	A/G	—	uncertain significance
rs376855597	2:219,507,688	C/T	—	uncertain significance
rs1697371244	2:219,507,725	G/A	—	pathogenic
rs369807902	2:219,507,737	G/A	—	uncertain significance
rs201712794	2:219,507,745	C/T	—	uncertain significance
rs200461087	2:219,507,748	G/T	—	uncertain significance
rs751102994	2:219,507,772	C/T	—	uncertain significance
rs756896397	2:219,507,773	G/A	—	uncertain significance
rs768106776	2:219,507,780	G/C	—	uncertain significance
rs150124453	2:219,507,793	G/A	—	uncertain significance
rs373958230	2:219,507,833	G/C	—	uncertain significance
rs1171379887	2:219,507,835	A/C	—	uncertain significance
rs779170335	2:219,507,844	G/C	—	uncertain significance
rs1378032328	2:219,507,929	A/C	—	uncertain significance
rs779082032	2:219,507,935	C/T	—	uncertain significance
rs747130010	2:219,507,979	C/T	—	likely benign
rs371282409	2:219,508,030	G/A	—	uncertain significance
rs546151500	2:219,508,064	G/A	—	pathogenic
rs188997501	2:219,508,077	G/A	—	likely benign
rs200582262	2:219,508,081	C/T	—	uncertain significance
rs367708840	2:219,508,082	G/A	—	uncertain significance
rs61733642	2:219,508,089	C/G	—	uncertain significance
rs202023725	2:219,508,118	T/G	—	uncertain significance
rs2469674038	2:219,508,139	G/A	—	uncertain significance
rs2469674439	2:219,508,171	T/C	—	uncertain significance
rs1697430338	2:219,508,177	A/C	—	uncertain significance
rs201639604	2:219,508,199	C/T	—	uncertain significance
rs1404251386	2:219,508,201	G/A	—	uncertain significance
rs61733644	2:219,508,211	A/G	—	benign
rs774611541	2:219,508,225	G/A	—	uncertain significance
rs200756709	2:219,508,253	G/A	—	uncertain significance
rs369246607	2:219,508,260	C/T	—	likely benign
rs199618335	2:219,508,261	G/A	—	uncertain significance
rs3770212	2:219,508,263	G/T	—	benign
rs1362873276	2:219,508,266	T/A	—	likely benign
rs61733645	2:219,508,287	G/A	—	benign
rs3770213	2:219,508,372	A/T	—	benign
rs2469678927	2:219,508,493	G/C	—	uncertain significance

Showing 100 of 208 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.