ClinVar Miner

List of variants in gene MAPT reported as benign for not provided

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Gene type:
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Total variants: 80
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HGVS dbSNP gnomAD frequency
NM_001377265.1(MAPT):c.1546T>C (p.Tyr516His) rs2258689 0.21570
NM_001377265.1(MAPT):c.1941T>C (p.Asn647=) rs17652121 0.14693
NM_001377265.1(MAPT):c.1091T>C (p.Val364Ala) rs62063787 0.14671
NM_001377265.1(MAPT):c.220+2535A>G rs1800547 0.14618
NM_001377265.1(MAPT):c.220+18C>T rs75242405 0.14617
NM_001377265.1(MAPT):c.-13A>G rs17650901 0.14470
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.1078G>A (p.Asp360Asn) rs62063786 0.12772
NM_001377265.1(MAPT):c.830C>T (p.Pro277Leu) rs63750417 0.12767
NM_001377265.1(MAPT):c.1564T>C (p.Ser522Pro) rs10445337 0.12766
NM_001377265.1(MAPT):c.1732+2342T>C rs62063845 0.12765
NM_001377265.1(MAPT):c.1704G>A (p.Pro568=) rs1052551 0.12440
NM_001377265.1(MAPT):c.1333C>T (p.Arg445Trp) rs17651549 0.12421
NM_001377265.1(MAPT):c.1080C>T (p.Asp360=) rs63750222 0.11265
NM_001377265.1(MAPT):c.1178C>T (p.Ser393Leu) rs73314997 0.05198
NM_001377265.1(MAPT):c.914A>G (p.Gln305Arg) rs63750072 0.03830
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.1708G>A (p.Ala570Thr) rs63750612 0.01415
NM_001377265.1(MAPT):c.896T>G (p.Val299Gly) rs141120474 0.00235
NM_001377265.1(MAPT):c.1630G>A (p.Ala544Thr) rs143624519 0.00179
NM_001377265.1(MAPT):c.1732+2364C>T rs187760483 0.00178
NM_001377265.1(MAPT):c.2091+29G>A rs63751443 0.00175
NM_001377265.1(MAPT):c.1505C>T (p.Ser502Phe) rs143956882 0.00169
NM_001377265.1(MAPT):c.117G>A (p.Thr39=) rs63750529 0.00154
NM_001377265.1(MAPT):c.912C>G (p.Pro304=) rs142327009 0.00112
NM_001377265.1(MAPT):c.762G>A (p.Glu254=) rs185284364 0.00083
NM_001377265.1(MAPT):c.50C>T (p.Thr17Met) rs144611688 0.00080
NM_001377265.1(MAPT):c.120C>T (p.Asp40=) rs191362093 0.00067
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.*241dup rs55661512
NM_001377265.1(MAPT):c.-17-171G>T
NM_001377265.1(MAPT):c.-17-277A>G
NM_001377265.1(MAPT):c.-17-322C>T
NM_001377265.1(MAPT):c.133+284C>T
NM_001377265.1(MAPT):c.134-284_134-281del
NM_001377265.1(MAPT):c.134-287del
NM_001377265.1(MAPT):c.134-290_134-289insACCA
NM_001377265.1(MAPT):c.134-92T>C
NM_001377265.1(MAPT):c.1351+249A>C
NM_001377265.1(MAPT):c.1351+315del
NM_001377265.1(MAPT):c.1352-198G>A
NM_001377265.1(MAPT):c.1352-72T>C
NM_001377265.1(MAPT):c.1407+297_1407+298insCCCC
NM_001377265.1(MAPT):c.1407+298_1407+299insGGACAGTAAATGAAGGTGTGTTTGAAAACCAAC
NM_001377265.1(MAPT):c.1408-198G>A
NM_001377265.1(MAPT):c.1408-249C>T
NM_001377265.1(MAPT):c.1605+105T>C
NM_001377265.1(MAPT):c.1605+241G>A
NM_001377265.1(MAPT):c.1605+67A>G
NM_001377265.1(MAPT):c.1606-283G>A
NM_001377265.1(MAPT):c.1606-334A>G
NM_001377265.1(MAPT):c.1732+2137C>G
NM_001377265.1(MAPT):c.1732+228C>G
NM_001377265.1(MAPT):c.1732+246C>T
NM_001377265.1(MAPT):c.1733-26G>A
NM_001377265.1(MAPT):c.176C>T (p.Pro59Leu)
NM_001377265.1(MAPT):c.1998+103G>A
NM_001377265.1(MAPT):c.1999-168G>A
NM_001377265.1(MAPT):c.1999-176A>G
NM_001377265.1(MAPT):c.1999-47C>A
NM_001377265.1(MAPT):c.2074G>A (p.Val692Ile)
NM_001377265.1(MAPT):c.2173+196C>T
NM_001377265.1(MAPT):c.2173+34G>A
NM_001377265.1(MAPT):c.2173+90G>A
NM_001377265.1(MAPT):c.2174-257dup
NM_001377265.1(MAPT):c.2174-323T>G
NM_001377265.1(MAPT):c.220+2277C>G
NM_001377265.1(MAPT):c.220+2278T>G
NM_001377265.1(MAPT):c.220+2301A>G
NM_001377265.1(MAPT):c.220+239G>A
NM_001377265.1(MAPT):c.220+2613G>A
NM_001377265.1(MAPT):c.220+2698T>C
NM_001377265.1(MAPT):c.221-103T>A
NM_001377265.1(MAPT):c.221-94A>T
NM_001377265.1(MAPT):c.286+291C>G
NM_001377265.1(MAPT):c.303G>A (p.Pro101=)
NM_001377265.1(MAPT):c.547G>A (p.Glu183Lys)

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