ZNF407

zinc finger protein 407

Summary

This gene encodes a zinc finger protein whose exact function is not known. It may be involved in transcriptional regulation. Several alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2009]

Known Variants333 total

rsid	Position (GRCh37)	Alleles	Class	ClinVar
rs7243081	18:72,343,008	T/C	—	benign
rs762941748	18:72,343,016	A/G	—	conflicting classifications of pathogenicity
rs2511889912	18:72,343,045	A/G	—	uncertain significance
rs1599025215	18:72,343,056	A/T	—	likely benign
rs2511889972	18:72,343,061	A/G	—	uncertain significance
rs754424061	18:72,343,069	G/T	—	uncertain significance
rs375400480	18:72,343,071	C/T	—	likely benign
rs747714506	18:72,343,072	G/A	—	uncertain significance
rs766353143	18:72,343,150	T/C	—	uncertain significance
rs2511890405	18:72,343,151	C/G	—	uncertain significance
rs75994611	18:72,343,156	A/G	—	benign
rs183921097	18:72,343,159	G/T	—	uncertain significance
rs3794942	18:72,343,181	A/G	—	benign
rs186922813	18:72,343,187	A/T	—	uncertain significance
rs748374834	18:72,343,221	G/A	—	likely benign
rs927636244	18:72,343,241	A/G	—	uncertain significance
rs376621360	18:72,343,285	G/C	—	uncertain significance
rs200523805	18:72,343,292	T/A	—	likely benign
rs372507403	18:72,343,300	G/C	—	uncertain significance
rs375286661	18:72,343,366	C/G	—	conflicting classifications of pathogenicity
rs200498966	18:72,343,393	A/G	—	likely benign
rs200158544	18:72,343,402	G/T	—	likely benign
rs74861823	18:72,343,465	A/G	—	conflicting classifications of pathogenicity
rs1305024488	18:72,343,590	T/C	—	likely benign
rs1984097933	18:72,343,639	C/T	—	uncertain significance
rs780420064	18:72,343,655	G/T	—	uncertain significance
rs781180214	18:72,343,757	C/T	—	uncertain significance
rs575463875	18:72,343,783	C/T	—	uncertain significance
rs376114695	18:72,343,805	G/A	—	uncertain significance
rs769026348	18:72,343,878	T/C	—	likely benign
rs756785043	18:72,343,972	A/G	—	uncertain significance
rs115368653	18:72,344,002	G/A	—	benign
rs771137840	18:72,344,022	G/A	—	uncertain significance
rs77148611	18:72,344,052	G/A	—	likely benign
rs1386739479	18:72,344,075	C/T	—	uncertain significance
rs141778977	18:72,344,080	C/T	—	uncertain significance
rs147229491	18:72,344,091	T/C	—	likely benign
rs77518676	18:72,344,108	A/G	—	conflicting classifications of pathogenicity
rs745996763	18:72,344,123	A/G	—	likely benign
rs774202284	18:72,344,146	C/G	—	uncertain significance
rs201998501	18:72,344,159	T/G	—	likely benign
rs144421339	18:72,344,178	C/T	—	likely benign
rs370581948	18:72,344,193	C/T	—	benign
rs114313623	18:72,344,210	C/T	—	benign
rs3794941	18:72,344,223	T/C	—	benign
rs587780522	18:72,344,233	A/G	—	likely benign
rs17817969	18:72,344,238	C/T	—	benign
rs771815117	18:72,344,257	C/T	—	uncertain significance
rs116304324	18:72,344,261	G/A	—	conflicting classifications of pathogenicity
rs372418170	18:72,344,271	C/T	—	uncertain significance
rs772946096	18:72,344,337	T/G	—	uncertain significance
rs2511895492	18:72,344,351	T/C	—	uncertain significance
rs764787764	18:72,344,366	T/G	—	uncertain significance
rs918585995	18:72,344,372	C/A	—	uncertain significance
rs762625238	18:72,344,383	A/G	—	uncertain significance
rs368834630	18:72,344,421	G/A	—	likely benign
rs776451413	18:72,344,423	G/C	—	uncertain significance
rs565191332	18:72,344,443	T/A	—	uncertain significance
rs774023666	18:72,344,454	C/A	—	likely benign
rs780972850	18:72,344,494	C/T	—	uncertain significance
rs573257833	18:72,344,495	G/A	—	likely benign
rs191767705	18:72,344,496	T/G	—	likely benign
rs77006793	18:72,344,498	C/T	—	likely benign
rs376677482	18:72,344,501	C/T	—	uncertain significance
rs373519575	18:72,344,505	C/T	—	uncertain significance
rs7227263	18:72,344,509	G/A	—	benign
rs7227391	18:72,344,553	G/A	—	benign
rs781554422	18:72,344,575	G/A	—	uncertain significance
rs1165851626	18:72,344,588	C/T	—	uncertain significance
rs759921804	18:72,344,614	G/A	—	uncertain significance
rs527983284	18:72,344,639	T/C	—	uncertain significance
rs777421915	18:72,344,710	A/C	—	likely benign
rs753726742	18:72,344,786	G/C	—	uncertain significance
rs183172085	18:72,344,816	A/G	—	uncertain significance
rs756960606	18:72,344,831	C/G	—	uncertain significance
rs774946239	18:72,344,882	C/G	—	uncertain significance
rs187139901	18:72,344,883	C/T	—	likely benign
rs139800364	18:72,344,902	T/C	—	likely benign
rs191782884	18:72,344,914	A/G	—	uncertain significance
rs149806516	18:72,344,966	G/T	—	conflicting classifications of pathogenicity
rs745462253	18:72,344,972	T/C	—	uncertain significance
rs1555670651	18:72,344,996	C/T	—	uncertain significance
rs531446199	18:72,345,050	G/A	—	uncertain significance
rs199577995	18:72,345,133	C/T	—	uncertain significance
rs369448284	18:72,345,137	C/T	—	uncertain significance
rs745947982	18:72,345,154	C/T	—	uncertain significance
rs377540468	18:72,345,179	T/C	—	uncertain significance
rs2511899361	18:72,345,200	A/C	—	uncertain significance
rs797046126	18:72,345,210	C/T	—	uncertain significance
rs200573495	18:72,345,267	A/G	—	likely benign
rs182062444	18:72,345,352	G/A	—	uncertain significance
rs1240491377	18:72,345,364	A/C	—	uncertain significance
rs767939879	18:72,345,393	A/G	—	likely benign
rs750895107	18:72,345,400	T/C	—	uncertain significance
rs202084477	18:72,345,468	T/A	—	uncertain significance
rs118088241	18:72,345,525	G/A	—	benign
rs377128271	18:72,345,527	C/T	—	uncertain significance
rs2511900898	18:72,345,563	C/T	—	uncertain significance
rs373567219	18:72,345,594	C/T	—	likely benign
rs368869230	18:72,345,692	G/A	—	uncertain significance

Showing 100 of 333 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.