List of variants in gene ADAMTS10 reported as benign for acromelic dysplasia

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: 21

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_030957.4(ADAMTS10):c.3303T>G (p.His1101Gln)	rs7252299	0.99986
NM_030957.4(ADAMTS10):c.1588-179G>T	rs9749567	0.92646
NM_030957.4(ADAMTS10):c.401= (p.Ser134=)	rs7255721	0.79500
NM_030957.4(ADAMTS10):c.2283T>C (p.Pro761=)	rs4476282	0.23173
NM_030957.4(ADAMTS10):c.*428A>G	rs116024095	0.07160
NM_030957.4(ADAMTS10):c.3102G>A (p.Thr1034=)	rs10405956	0.03322
NM_030957.4(ADAMTS10):c.2584G>T (p.Ala862Ser)	rs10418929	0.03247
NM_030957.4(ADAMTS10):c.1900+11G>C	rs78421590	0.02958
NM_030957.4(ADAMTS10):c.185G>A (p.Arg62Gln)	rs62621197	0.02952
NM_030957.4(ADAMTS10):c.1588-7C>G	rs11882422	0.02550
NM_030957.4(ADAMTS10):c.*449G>C	rs555471852	0.01330
NM_030957.4(ADAMTS10):c.1350G>T (p.Gly450=)	rs75734496	0.01217
NM_030957.4(ADAMTS10):c.1803T>C (p.Cys601=)	rs115093676	0.00762
NM_030957.4(ADAMTS10):c.*259G>A	rs74498506	0.00739
NM_030957.4(ADAMTS10):c.3193G>A (p.Gly1065Ser)	rs80046653	0.00659
NM_030957.4(ADAMTS10):c.2865+11C>A	rs367808475	0.00505
NM_030957.4(ADAMTS10):c.356G>A (p.Arg119Gln)	rs3814291	0.00472
NM_030957.4(ADAMTS10):c.204G>A (p.Thr68=)	rs139761152	0.00397
NM_030957.4(ADAMTS10):c.*20G>A	rs137928083	0.00385
NM_030957.4(ADAMTS10):c.1901-11G>A	rs117220199	0.00106
NM_030957.4(ADAMTS10):c.811-149G>A	rs7248483

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.