List of variants in gene MAPT reported as likely pathogenic

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: 9

Download table as spreadsheet

HGVS	dbSNP
NM_001377265.1(MAPT):c.2014AAG[1] (p.Lys673del)	rs63750688
NM_001377265.1(MAPT):c.2064T>C (p.Asn688=)	rs63750912
NM_001377265.1(MAPT):c.2091+19C>G	rs63750162
NM_001377265.1(MAPT):c.2228A>G (p.Gln743Arg)	rs1568339821
NM_001377265.1(MAPT):c.2242T>A (p.Ser748Thr)	rs2076339915
NM_001377265.1(MAPT):c.2260C>T (p.His754Tyr)	rs1568339995
NM_001377265.1(MAPT):c.2263G>A (p.Val755Ile)	rs63750869
NM_001377265.1(MAPT):c.2266C>A (p.Pro756Thr)	rs1598408336
NM_001377265.1(MAPT):c.2341G>A (p.Gly781Arg)	rs63750512

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.