List of variants in gene DSTYK reported as benign for not provided

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 31

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NC_000001.11:g.205211934T>C	rs2369633	0.93551
NM_015375.3(DSTYK):c.1921T>C (p.Cys641Arg)	rs3851294	0.93525
NM_015375.3(DSTYK):c.1558-244T>C	rs6684220	0.91717
NM_015375.3(DSTYK):c.266-174T>C	rs6593929	0.78717
NM_015375.3(DSTYK):c.266-166A>G	rs10900464	0.45199
NM_015375.3(DSTYK):c.2028C>T (p.Phe676=)	rs1062715	0.29534
NM_015375.3(DSTYK):c.*51T>A	rs11367	0.25165
NM_015375.3(DSTYK):c.1558-217_1558-216insT	rs34880166	0.17671
NM_015375.3(DSTYK):c.2467+245del	rs67001092	0.17505
NM_015375.3(DSTYK):c.2467+227G>A	rs12120595	0.17493
NM_015375.3(DSTYK):c.2353-59G>A	rs3851295	0.14875
NM_015375.3(DSTYK):c.1325-86A>G	rs61822658	0.07918
NM_015375.3(DSTYK):c.1294C>G (p.Leu432Val)	rs35845538	0.03231
NM_015375.3(DSTYK):c.655-30C>T	rs76346293	0.02510
NM_015375.3(DSTYK):c.1557+220C>T	rs113428324	0.02412
NM_015375.3(DSTYK):c.190C>T (p.Leu64Phe)	rs78212113	0.02402
NM_015375.3(DSTYK):c.2239-205G>T	rs141235885	0.01274
NM_015375.3(DSTYK):c.1557+9A>C	rs79995334	0.00935
NM_015375.3(DSTYK):c.1209A>G (p.Glu403=)	rs35208779	0.00908
NM_015375.3(DSTYK):c.1677C>T (p.Ala559=)	rs34830650	0.00268
NM_015375.3(DSTYK):c.2105+10G>A	rs200576489	0.00131
NM_015375.3(DSTYK):c.655-8C>T	rs201628576	0.00053
NM_015375.3(DSTYK):c.53C>T (p.Pro18Leu)	rs202068245	0.00047
NM_015375.3(DSTYK):c.120G>T (p.Arg40=)	rs201374829	0.00018
NM_015375.3(DSTYK):c.1542T>C (p.Ser514=)	rs146330673	0.00018
NM_015375.3(DSTYK):c.1384C>A (p.Arg462=)	rs77626160
NM_015375.3(DSTYK):c.1558-224dup	rs373494891
NM_015375.3(DSTYK):c.1642-20C>T
NM_015375.3(DSTYK):c.1818+95GT[6]	rs10631913
NM_015375.3(DSTYK):c.2603-181dup	rs35284794
NM_015375.3(DSTYK):c.42G>C (p.Ser14=)	rs140909469

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.