ClinVar Miner

List of variants in gene MAPT reported as uncertain significance by Illumina Laboratory Services,Illumina

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 62
Download table as spreadsheet
HGVS dbSNP
NM_001377265.1(MAPT):c.*1089G>A rs2076756072
NM_001377265.1(MAPT):c.*1108G>A rs886053036
NM_001377265.1(MAPT):c.*1108G>T rs886053036
NM_001377265.1(MAPT):c.*1145C>T rs1282124024
NM_001377265.1(MAPT):c.*1248T>G rs1359343408
NM_001377265.1(MAPT):c.*1464C>T rs886053037
NM_001377265.1(MAPT):c.*1603C>A rs62062298
NM_001377265.1(MAPT):c.*1671A>C rs2076783375
NM_001377265.1(MAPT):c.*1737del rs886053038
NM_001377265.1(MAPT):c.*1864T>C rs1045372663
NM_001377265.1(MAPT):c.*1889T>G rs886053039
NM_001377265.1(MAPT):c.*1892A>C rs886053040
NM_001377265.1(MAPT):c.*1910G>C rs886053041
NM_001377265.1(MAPT):c.*1910G>T rs886053041
NM_001377265.1(MAPT):c.*1933_*1936del rs886053042
NM_001377265.1(MAPT):c.*1960G>A rs372196788
NM_001377265.1(MAPT):c.*2122G>A rs534237172
NM_001377265.1(MAPT):c.*2186C>A rs2076806697
NM_001377265.1(MAPT):c.*2251C>T rs886053043
NM_001377265.1(MAPT):c.*2252G>A rs1408084649
NM_001377265.1(MAPT):c.*2288_*2289inv
NM_001377265.1(MAPT):c.*242A>T rs3209489
NM_001377265.1(MAPT):c.*2493G>A rs886053044
NM_001377265.1(MAPT):c.*250dup rs1555726075
NM_001377265.1(MAPT):c.*2527C>A rs916922460
NM_001377265.1(MAPT):c.*2531AGGA[1] rs886053045
NM_001377265.1(MAPT):c.*2636G>A rs2076822793
NM_001377265.1(MAPT):c.*2681C>G rs886053047
NM_001377265.1(MAPT):c.*2737G>C rs886053048
NM_001377265.1(MAPT):c.*2857G>A rs886053049
NM_001377265.1(MAPT):c.*2931G>C rs536017906
NM_001377265.1(MAPT):c.*2969G>A rs886053050
NM_001377265.1(MAPT):c.*3004T>C rs886053051
NM_001377265.1(MAPT):c.*412G>C rs886053033
NM_001377265.1(MAPT):c.*453T>G rs570856603
NM_001377265.1(MAPT):c.*524G>A rs886053034
NM_001377265.1(MAPT):c.*537G>A rs2076731366
NM_001377265.1(MAPT):c.*553G>A rs1053380107
NM_001377265.1(MAPT):c.*670G>A rs753718859
NM_001377265.1(MAPT):c.*734C>G rs1190546785
NM_001377265.1(MAPT):c.*785A>G rs563116941
NM_001377265.1(MAPT):c.*844C>T rs886053035
NM_001377265.1(MAPT):c.*852C>T rs548424713
NM_001377265.1(MAPT):c.*857G>A rs1043283500
NM_001377265.1(MAPT):c.*884G>A rs1255580984
NM_001377265.1(MAPT):c.-141G>A rs886053027
NM_001377265.1(MAPT):c.-26G>T rs886053029
NM_001377265.1(MAPT):c.162C>T (p.Asp54=) rs750428288
NM_001377265.1(MAPT):c.1972C>T (p.Leu658=) rs63750349
NM_001377265.1(MAPT):c.2173+9G>C rs979650971
NM_001377265.1(MAPT):c.220+2538C>G rs368845248
NM_001377265.1(MAPT):c.221C>G (p.Ala74Gly) rs886053030
NM_001377265.1(MAPT):c.2271C>T (p.Gly757=) rs148501218
NM_001377265.1(MAPT):c.2319C>T (p.Asn773=) rs746312281
NM_005910.5(MAPT):c.-163G>T rs886053026
NM_005910.5(MAPT):c.-177G>C rs886053025
NM_005910.5(MAPT):c.-235C>G rs550530601
NM_005910.5(MAPT):c.-241C>T rs1021756382
NM_005910.5(MAPT):c.-245C>T rs886053024
NM_005910.5(MAPT):c.-310G>T rs886053023
NM_005910.5(MAPT):c.-314G>A rs886053022
NM_005910.5(MAPT):c.-315C>A rs886053021

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.