CHD1L

chromodomain helicase DNA binding protein 1 like

Summary

This gene encodes a DNA helicase protein involved in DNA repair. The protein converts ATP to add poly(ADP-ribose) as it regulates chromatin relaxation following DNA damage. Overexpression of this gene has been linked to several types of cancers. [provided by RefSeq, Feb 2017]

Known Variants162 total

rsid	Position (GRCh37)	Alleles	Class	ClinVar
rs72997588	1:146,714,091	G/T	—	benign
rs72997590	1:146,714,213	C/T	—	benign
rs1890040	1:146,714,255	A/G	—	benign
rs1890041	1:146,714,281	C/G	—	benign
rs147494800	1:146,714,354	A/T	—	likely benign
rs1665087556	1:146,714,370	C/G	—	uncertain significance
rs373271315	1:146,714,376	G/T	—	likely benign
rs781885928	1:146,714,381	G/C	—	uncertain significance
rs782416368	1:146,714,388	A/G	—	uncertain significance
rs587765929	1:146,714,389	A/G	—	likely benign
rs1890042	1:146,714,392	G/C	—	benign
rs782152009	1:146,714,400	T/A	—	uncertain significance
rs11588753	1:146,714,427	G/C	—	benign
rs1890043	1:146,714,588	C/T	—	benign
rs57078845	1:146,722,222	G/A	intron variant	—
rs59689207	1:146,722,484	G/A	intron variant	—
rs1890038	1:146,723,941	C/T	—	benign
rs3820130	1:146,724,003	A/G	—	benign
rs1890037	1:146,724,093	A/G	—	benign
rs3737844	1:146,724,321	C/T	—	likely benign
rs1553937318	1:146,724,376	G/T	—	uncertain significance
rs1311096135	1:146,724,384	C/T	—	uncertain significance
rs2526336253	1:146,724,386	G/T	—	uncertain significance
rs3737845	1:146,724,408	G/A	—	benign
rs72999632	1:146,726,176	T/C	—	benign
rs370027194	1:146,726,591	C/T	—	uncertain significance
rs7548820	1:146,726,846	G/A	—	benign
rs28706431	1:146,727,128	C/T	—	benign
rs6696488	1:146,727,178	G/A	—	benign
rs17160050	1:146,727,213	T/C	—	benign
rs17160051	1:146,727,388	G/T	—	benign
rs1553939952	1:146,727,533	A/C	—	uncertain significance
rs201680696	1:146,727,553	C/T	—	uncertain significance
rs1669968602	1:146,727,579	T/G	—	uncertain significance
rs3737846	1:146,727,593	G/A	—	benign
rs1932978	1:146,727,763	G/A	—	benign
rs12119390	1:146,728,149	A/G	—	benign
rs782146681	1:146,728,185	A/T	—	uncertain significance
rs72999634	1:146,730,896	A/C	—	—
rs41295829	1:146,731,813	C/T	—	benign
rs12751576	1:146,731,822	C/T	—	benign
rs72999639	1:146,735,811	T/C	—	benign
rs2526756594	1:146,736,091	T/C	—	uncertain significance
rs4950315	1:146,736,092	C/T	—	benign
rs587674066	1:146,736,109	C/T	—	uncertain significance
rs145790163	1:146,736,110	C/T	—	benign
rs1458109974	1:146,736,112	G/C	—	uncertain significance
rs143518204	1:146,736,128	C/G	—	uncertain significance
rs587632403	1:146,736,169	C/T	—	uncertain significance
rs78843378	1:146,736,176	C/G	—	benign
rs201333837	1:146,736,211	G/A	—	uncertain significance
rs2526761925	1:146,736,223	T/C	—	uncertain significance
rs4950392	1:146,736,548	G/T	—	benign
rs17356219	1:146,737,343	A/C	—	benign
rs10159076	1:146,737,357	G/T	—	benign
rs3737848	1:146,737,490	G/C	—	benign
rs782107935	1:146,737,613	G/T	—	uncertain significance
rs2526812011	1:146,737,663	C/T	—	uncertain significance
rs782537728	1:146,737,680	G/A	—	uncertain significance
rs886041164	1:146,737,685	A/G	—	uncertain significance
rs782669205	1:146,737,686	T/C	—	uncertain significance
rs111296687	1:146,737,700	A/C	—	benign
rs2526815116	1:146,737,720	A/G	—	uncertain significance
rs11239963	1:146,739,068	T/C	—	benign
rs149171266	1:146,739,075	T/A	—	likely benign
rs373036183	1:146,739,172	T/G	—	uncertain significance
rs4143738	1:146,739,277	T/C	—	benign
rs17356233	1:146,740,502	C/G	—	benign
rs377698659	1:146,740,533	T/C	—	uncertain significance
rs11576360	1:146,740,576	A/G	—	benign
rs12026756	1:146,742,351	C/T	—	benign
rs782774593	1:146,742,591	A/C	—	uncertain significance
rs1675947168	1:146,742,604	T/C	—	uncertain significance
rs3737855	1:146,742,918	G/A	—	benign
rs7536363	1:146,743,611	A/G	—	benign
rs782747449	1:146,743,928	T/C	—	uncertain significance
rs1676541454	1:146,743,931	G/A	—	uncertain significance
rs72999648	1:146,746,892	G/A	—	benign
rs2275250	1:146,747,069	T/C	—	benign
rs1553956777	1:146,747,083	A/G	—	uncertain significance
rs6680778	1:146,747,153	C/T	—	benign
rs6672850	1:146,747,232	C/T	—	benign
rs12023638	1:146,747,419	G/T	—	benign
rs11376734	1:146,747,461	A/A	—	benign
rs113139670	1:146,747,766	A/G	—	likely benign
rs200226258	1:146,747,797	G/A	—	uncertain significance
rs375996768	1:146,747,851	C/T	—	uncertain significance
rs367859293	1:146,747,901	G/A	—	uncertain significance
rs7534963	1:146,748,072	A/G	—	benign
rs17360443	1:146,751,410	C/A	—	benign
rs376783101	1:146,751,710	A/G	—	benign
rs782651981	1:146,751,754	C/T	—	uncertain significance
rs2527270474	1:146,751,756	A/G	—	uncertain significance
rs373424057	1:146,751,757	T/C	—	likely benign
rs7547279	1:146,751,782	A/C	—	benign
rs374644093	1:146,751,806	G/A	—	likely benign
rs72999655	1:146,755,784	A/G	—	benign
rs782302924	1:146,756,024	A/G	—	uncertain significance
rs1553963851	1:146,756,041	T/C	—	uncertain significance
rs782565499	1:146,756,099	A/C	—	uncertain significance

Showing 100 of 162 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.