List of variants in gene MAPT reported as likely benign by Illumina Laboratory Services,Illumina

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: 11

Download table as spreadsheet

HGVS	dbSNP
NM_001377265.1(MAPT):c.2616_2618dup	rs375986662
NM_001377265.1(MAPT):c.*49G>A	rs367621316
NM_001377265.1(MAPT):c.*65AAT[1]	rs564954259
NM_001377265.1(MAPT):c.14G>A (p.Arg5His)	rs63750959
NM_001377265.1(MAPT):c.1630G>A (p.Ala544Thr)	rs143624519
NM_001377265.1(MAPT):c.1632C>A (p.Ala544=)	rs757701420
NM_001377265.1(MAPT):c.1974G>A (p.Leu658=)	rs373081497
NM_001377265.1(MAPT):c.2079G>A (p.Pro693=)	rs63751395
NM_001377265.1(MAPT):c.220+2450A>G	rs773274633
NM_001377265.1(MAPT):c.2364G>A (p.Ser788=)	rs377720312
NM_001377265.1(MAPT):c.2457G>A (p.Thr819=)	rs369954009

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.