List of variants in gene MAPT reported as 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: 39

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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

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