List of variants reported as likely benign for Mastocytosis

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

Total variants: 11

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_000222.3(KIT):c.2586G>C (p.Leu862=)	rs3733542	0.16755
NM_000222.3(KIT):c.1621A>C (p.Met541Leu)	rs3822214	0.07727
NM_000222.3(KIT):c.*299G>C	rs185479436	0.00330
NM_000222.3(KIT):c.200C>G (p.Thr67Ser)	rs144933028	0.00045
NM_000222.3(KIT):c.67+12C>T	rs374618962	0.00031
NM_000222.3(KIT):c.2349C>T (p.Leu783=)	rs151046591	0.00022
NM_000222.3(KIT):c.1674G>A (p.Lys558=)	rs200375589	0.00016
NM_000222.3(KIT):c.2263G>A (p.Ala755Thr)	rs201165084	0.00013
NM_000222.3(KIT):c.464C>T (p.Pro155Leu)	rs367719489	0.00009
NM_000222.3(KIT):c.2802+9A>G	rs369450271	0.00004
NM_000222.3(KIT):c.252G>T (p.Thr84=)	rs56411694

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.