ClinVar Miner

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

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 37
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HGVS dbSNP
NM_001377265.1(MAPT):c.*1206AC[1] rs66561280
NM_001377265.1(MAPT):c.*1328A>C rs17574040
NM_001377265.1(MAPT):c.*1396T>C rs16940799
NM_001377265.1(MAPT):c.*1909_*1910del rs71760839
NM_001377265.1(MAPT):c.*2288T>C rs75010486
NM_001377265.1(MAPT):c.*2289G>A rs16940806
NM_001377265.1(MAPT):c.*2390_*2391insT rs35134656
NM_001377265.1(MAPT):c.*241dup rs55661512
NM_001377265.1(MAPT):c.*26T>C rs9468
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.*334A>G rs8712
NM_001377265.1(MAPT):c.*464G>A rs17574005
NM_001377265.1(MAPT):c.*732C>A rs189413478
NM_001377265.1(MAPT):c.*76G>A rs73317038
NM_001377265.1(MAPT):c.*907CT[3] rs56289286
NM_001377265.1(MAPT):c.-133C>A rs62056779
NM_001377265.1(MAPT):c.-13A>G rs17650901
NM_001377265.1(MAPT):c.-42del rs144722105
NM_001377265.1(MAPT):c.13C>T (p.Arg5Cys) rs766166210
NM_001377265.1(MAPT):c.1638G>A (p.Pro546=) rs201046056
NM_001377265.1(MAPT):c.1670A>G (p.Gln557Arg) rs568067396
NM_001377265.1(MAPT):c.1704G>A (p.Pro568=) rs1052551
NM_001377265.1(MAPT):c.1708G>A (p.Ala570Thr) rs63750612
NM_001377265.1(MAPT):c.1776C>T (p.Pro592=) rs201057449
NM_001377265.1(MAPT):c.1801C>T (p.Arg601Cys) rs138984221
NM_001377265.1(MAPT):c.1802G>A (p.Arg601His) rs115492908
NM_001377265.1(MAPT):c.1857A>G (p.Ala619=) rs1052553
NM_001377265.1(MAPT):c.1891G>A (p.Ala631Thr) rs63750096
NM_001377265.1(MAPT):c.1938G>A (p.Lys646=) rs141636979
NM_001377265.1(MAPT):c.1941T>C (p.Asn647=) rs17652121
NM_001377265.1(MAPT):c.1986G>A (p.Pro662=) rs11568305
NM_001377265.1(MAPT):c.220+2503C>T rs138293088
NM_001377265.1(MAPT):c.220+2535A>G rs1800547
NM_005910.5(MAPT):c.-285A>G rs11575895

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