DSTYK

dual serine/threonine and tyrosine protein kinase

Summary

This gene encodes a dual serine/threonine and tyrosine protein kinase which is expressed in multiple tissues. It is thought to function as a regulator of cell death. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2008]

Known Variants206 total

rsid	Position (GRCh37)	Alleles	Class	ClinVar
rs12137465	1:205,114,665	G/T	—	—
rs11367	1:205,116,635	A/T	—	benign
rs146033090	1:205,116,694	A/T	—	uncertain significance
rs148542303	1:205,116,700	C/A	—	uncertain significance
rs370809794	1:205,116,709	T/C	—	uncertain significance
rs1411730987	1:205,116,714	G/C	—	uncertain significance
rs939944869	1:205,116,721	C/G	—	uncertain significance
rs151054719	1:205,116,729	G/A	—	likely benign
rs2526765322	1:205,116,751	T/C	—	uncertain significance
rs1657276571	1:205,116,758	G/A	—	likely benign
rs562344996	1:205,116,760	G/A	—	uncertain significance
rs2102372872	1:205,116,775	T/C	—	uncertain significance
rs774879238	1:205,116,776	G/A	—	uncertain significance
rs761744798	1:205,116,803	G/A	—	likely benign
rs368296430	1:205,116,858	C/T	—	uncertain significance
rs1574742379	1:205,116,871	C/A	—	uncertain significance
rs777906531	1:205,116,872	C/G	—	likely benign
rs778586547	1:205,117,407	G/A	—	uncertain significance
rs1308806650	1:205,117,416	T/C	—	uncertain significance
rs12120595	1:205,119,581	C/T	—	benign
rs2526778526	1:205,119,802	C/T	—	uncertain significance
rs1657377901	1:205,119,865	T/C	—	uncertain significance
rs773130126	1:205,119,907	G/A	—	uncertain significance
rs3851295	1:205,119,981	C/T	—	benign
rs150021641	1:205,124,049	C/T	intron variant	—
rs111507314	1:205,126,404	C/A	—	likely benign
rs142354055	1:205,126,452	G/C	—	uncertain significance
rs2526807201	1:205,126,460	T/C	—	uncertain significance
rs2526807549	1:205,126,495	G/A	—	uncertain significance
rs1351795306	1:205,126,513	G/C	—	uncertain significance
rs184840693	1:205,126,532	G/C	—	likely benign
rs141235885	1:205,126,719	A/C	—	benign
rs2102396676	1:205,128,695	C/T	—	uncertain significance
rs369367865	1:205,128,697	C/T	—	conflicting classifications of pathogenicity
rs114762711	1:205,128,698	G/A	—	likely benign
rs755781145	1:205,128,706	C/T	—	uncertain significance
rs150778354	1:205,128,707	G/A	—	uncertain significance
rs373307614	1:205,128,716	T/C	—	uncertain significance
rs56147706	1:205,128,751	T/C	—	conflicting classifications of pathogenicity
rs770207646	1:205,128,765	T/C	—	likely benign
rs200118459	1:205,128,798	C/T	—	likely benign
rs201385262	1:205,128,799	G/A	—	uncertain significance
rs919938431	1:205,128,814	G/A	—	likely benign
rs1657662208	1:205,128,819	G/A	—	likely benign
rs200576489	1:205,129,232	C/T	—	benign
rs776078988	1:205,129,278	T/C	—	uncertain significance
rs1062715	1:205,129,319	G/A	—	benign
rs1035239987	1:205,129,368	C/T	—	uncertain significance
rs1460909694	1:205,129,378	C/G	—	uncertain significance
rs147872876	1:205,129,388	T/A	—	uncertain significance
rs776132078	1:205,129,398	C/T	—	uncertain significance
rs370797486	1:205,129,417	G/C	—	likely benign
rs572194692	1:205,129,924	T/C	—	—
rs3851294	1:205,130,413	A/G	—	benign
rs2526826522	1:205,130,419	C/T	—	uncertain significance
rs774289190	1:205,130,430	C/T	—	uncertain significance
rs535442055	1:205,130,439	C/T	—	uncertain significance
rs767625627	1:205,130,440	G/A	—	uncertain significance
rs765391969	1:205,130,457	C/T	—	uncertain significance
rs758632426	1:205,130,464	T/A	—	uncertain significance
rs146470052	1:205,130,473	G/T	—	uncertain significance
rs374722933	1:205,130,481	G/A	—	uncertain significance
rs1300122167	1:205,130,494	G/A	—	uncertain significance
rs367692056	1:205,130,518	G/A	—	conflicting classifications of pathogenicity
rs867889224	1:205,131,180	G/A	—	uncertain significance
rs147801354	1:205,131,188	C/T	—	likely benign
rs764647986	1:205,131,191	G/A	—	likely benign
rs148815814	1:205,131,207	C/T	—	conflicting classifications of pathogenicity
rs148048922	1:205,131,208	G/A	—	uncertain significance
rs371839746	1:205,131,209	A/T	—	likely benign
rs374851853	1:205,131,222	C/G	—	uncertain significance
rs147190858	1:205,131,251	G/A	—	likely benign
rs1342003682	1:205,131,301	T/A	—	uncertain significance
rs34830650	1:205,131,305	G/C	—	likely benign
rs530895091	1:205,131,360	G/A	—	benign
rs771221493	1:205,132,035	A/G	—	likely benign
rs756860232	1:205,132,060	T/C	—	likely benign
rs1301300372	1:205,132,080	T/A	—	uncertain significance
rs567099854	1:205,132,148	C/T	—	likely benign
rs6684220	1:205,132,378	A/G	—	benign
rs113428324	1:205,132,631	G/A	—	benign
rs79995334	1:205,132,842	T/G	—	benign
rs146330673	1:205,132,866	A/G	—	likely benign
rs2526841062	1:205,132,886	C/T	—	uncertain significance
rs746112821	1:205,132,931	C/A	—	likely pathogenic
rs770083231	1:205,132,932	G/C	—	likely benign
rs549617235	1:205,132,944	C/T	—	likely benign
rs569664059	1:205,132,972	T/G	—	uncertain significance
rs760338678	1:205,132,990	T/G	—	uncertain significance
rs774752814	1:205,132,996	C/T	—	uncertain significance
rs1293987261	1:205,133,003	T/C	—	uncertain significance
rs2526841964	1:205,133,014	T/C	—	likely pathogenic
rs77626160	1:205,133,024	G/T	—	conflicting classifications of pathogenicity
rs780304861	1:205,133,034	T/C	—	likely benign
rs368372837	1:205,133,039	T/G	—	uncertain significance
rs2526842392	1:205,133,073	G/A	—	likely benign
rs372309264	1:205,133,082	G/C	—	uncertain significance
rs61822658	1:205,133,169	T/C	—	benign
rs11240373	1:205,135,600	A/C	intron variant	—
rs35845538	1:205,138,321	G/C	—	benign

Showing 100 of 206 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.