ClinVar Miner

List of variants in gene MAPT reported as benign for MAPT-Related Spectrum Disorders

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 39
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_001377265.1(MAPT):c.*3858A>G rs7521 0.56139
NM_001377265.1(MAPT):c.1941T>C (p.Asn647=) rs17652121 0.14693
NM_001377265.1(MAPT):c.220+2535A>G rs1800547 0.14618
NM_005910.5(MAPT):c.-285A>G rs11575895 0.14499
NM_001377265.1(MAPT):c.-133C>A rs62056779 0.14475
NM_001377265.1(MAPT):c.-13A>G rs17650901 0.14470
NM_001377265.1(MAPT):c.*1328A>C rs17574040 0.14462
NM_001377265.1(MAPT):c.*2288T>C rs75010486 0.14444
NM_001377265.1(MAPT):c.*2289G>A rs16940806 0.14437
NM_001377265.1(MAPT):c.*1909_*1910del rs71760839 0.14410
NM_001377265.1(MAPT):c.1857A>G (p.Ala619=) rs1052553 0.12790
NM_001377265.1(MAPT):c.*26T>C rs9468 0.12782
NM_001377265.1(MAPT):c.*334A>G rs8712 0.12761
NM_001377265.1(MAPT):c.*2390_*2391insT rs35134656 0.12519
NM_001377265.1(MAPT):c.*1396T>C rs16940799 0.12478
NM_001377265.1(MAPT):c.1704G>A (p.Pro568=) rs1052551 0.12440
NM_001377265.1(MAPT):c.1986G>A (p.Pro662=) rs11568305 0.03713
NM_001377265.1(MAPT):c.*76G>A rs73317038 0.02995
NM_001377265.1(MAPT):c.*464G>A rs17574005 0.01741
NM_001377265.1(MAPT):c.1708G>A (p.Ala570Thr) rs63750612 0.01415
NM_001377265.1(MAPT):c.*732C>A rs189413478 0.00262
NM_001377265.1(MAPT):c.*3951G>A rs368485438 0.00192
NM_001377265.1(MAPT):c.1891G>A (p.Ala631Thr) rs63750096 0.00067
NM_001377265.1(MAPT):c.1938G>A (p.Lys646=) rs141636979 0.00009
NM_001377265.1(MAPT):c.1801C>T (p.Arg601Cys) rs138984221 0.00006
NM_001377265.1(MAPT):c.1802G>A (p.Arg601His) rs115492908 0.00006
NM_001377265.1(MAPT):c.1638G>A (p.Pro546=) rs201046056 0.00004
NM_001377265.1(MAPT):c.220+2503C>T rs138293088 0.00002
NM_001377265.1(MAPT):c.13C>T (p.Arg5Cys) rs766166210 0.00001
NM_001377265.1(MAPT):c.1670A>G (p.Gln557Arg) rs568067396 0.00001
NM_001377265.1(MAPT):c.1776C>T (p.Pro592=) rs201057449 0.00001
NM_001377265.1(MAPT):c.*1206AC[1] rs66561280
NM_001377265.1(MAPT):c.*241dup rs55661512
NM_001377265.1(MAPT):c.*2743del rs5820606
NM_001377265.1(MAPT):c.*2876_*2878del rs35654420
NM_001377265.1(MAPT):c.*3040CTT[1] rs67656733
NM_001377265.1(MAPT):c.*317dup rs55658521
NM_001377265.1(MAPT):c.*907CT[3] rs56289286
NM_001377265.1(MAPT):c.-42del rs144722105

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.