ClinVar Miner

List of variants in gene MAPT reported as likely benign

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Gene type:
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Total variants: 167
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HGVS dbSNP gnomAD frequency
NM_001377265.1(MAPT):c.1178C>T (p.Ser393Leu) rs73314997 0.05622
NM_001377265.1(MAPT):c.914A>G (p.Gln305Arg) rs63750072 0.03830
NM_001377265.1(MAPT):c.220+2202G>A rs112165071 0.01404
NM_001377265.1(MAPT):c.1733-31T>C rs112663614 0.01201
NM_001377265.1(MAPT):c.-17-215C>T rs145236675 0.01116
NM_001377265.1(MAPT):c.862G>A (p.Gly288Arg) rs76375268 0.01093
NM_001377265.1(MAPT):c.1351+21C>T rs113608413 0.01091
NM_001377265.1(MAPT):c.2286+109G>C rs141893234 0.01084
NM_001377265.1(MAPT):c.1352-103C>T rs114859001 0.01077
NM_001377265.1(MAPT):c.2092-192C>T rs118109282 0.00672
NM_001377265.1(MAPT):c.1998+147C>T rs190722319 0.00571
NM_001377265.1(MAPT):c.1732+195C>A rs114790373 0.00546
NM_001377265.1(MAPT):c.464G>A (p.Arg155His) rs116395699 0.00502
NM_001377265.1(MAPT):c.427G>T (p.Ala143Ser) rs114203446 0.00484
NM_001377265.1(MAPT):c.896T>G (p.Val299Gly) rs141120474 0.00235
NM_001377265.1(MAPT):c.1628T>C (p.Ile543Thr) rs114635790 0.00217
NM_001377265.1(MAPT):c.2091+29G>A rs63751443 0.00213
NM_001377265.1(MAPT):c.1732+2364C>T rs187760483 0.00195
NM_001377265.1(MAPT):c.1630G>A (p.Ala544Thr) rs143624519 0.00179
NM_001377265.1(MAPT):c.1505C>T (p.Ser502Phe) rs143956882 0.00160
NM_001377265.1(MAPT):c.117G>A (p.Thr39=) rs63750529 0.00154
NM_001377265.1(MAPT):c.2074G>A (p.Val692Ile) rs116733906 0.00116
NM_001377265.1(MAPT):c.912C>G (p.Pro304=) rs142327009 0.00112
NM_001377265.1(MAPT):c.1891G>A (p.Ala631Thr) rs63750096 0.00085
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.1351+52C>T rs374352873 0.00041
NM_001377265.1(MAPT):c.889C>A (p.Arg297Ser) rs150983093 0.00038
NM_001377265.1(MAPT):c.777C>T (p.Ala259=) rs370558032 0.00027
NM_001377265.1(MAPT):c.774C>T (p.His258=) rs761089103 0.00026
NM_001377265.1(MAPT):c.54C>T (p.Tyr18=) rs63750811 0.00024
NM_001377265.1(MAPT):c.1998+15C>T rs749726538 0.00019
NM_001377265.1(MAPT):c.273T>C (p.Gly91=) rs141556635 0.00019
NM_001377265.1(MAPT):c.643C>T (p.Pro215Ser) rs151115928 0.00019
NM_001377265.1(MAPT):c.1854G>A (p.Val618=) rs114900761 0.00018
NM_001377265.1(MAPT):c.1326C>T (p.Pro442=) rs201312701 0.00017
NM_001377265.1(MAPT):c.921C>G (p.Ser307=) rs147885393 0.00017
NM_001377265.1(MAPT):c.1070C>T (p.Ser357Leu) rs199644237 0.00014
NM_001377265.1(MAPT):c.2262C>T (p.His754=) rs747658161 0.00013
NM_001377265.1(MAPT):c.1567C>T (p.Arg523Ter) rs200099007 0.00011
NM_001377265.1(MAPT):c.2349G>A (p.Glu783=) rs142776675 0.00011
NM_001377265.1(MAPT):c.678C>T (p.Ser226=) rs537438059 0.00011
NM_001377265.1(MAPT):c.2079G>A (p.Pro693=) rs63751395 0.00010
NM_001377265.1(MAPT):c.1137C>T (p.His379=) rs142283842 0.00009
NM_001377265.1(MAPT):c.1623G>A (p.Thr541=) rs139748238 0.00009
NM_001377265.1(MAPT):c.1938G>A (p.Lys646=) rs141636979 0.00009
NM_001377265.1(MAPT):c.*49G>A rs367621316 0.00008
NM_001377265.1(MAPT):c.1676A>G (p.Asn559Ser) rs150420625 0.00007
NM_001377265.1(MAPT):c.2271C>T (p.Gly757=) rs148501218 0.00007
NM_001377265.1(MAPT):c.176C>T (p.Pro59Leu) rs143138715 0.00006
NM_001377265.1(MAPT):c.220+2480G>A rs368318765 0.00006
NM_001377265.1(MAPT):c.80G>A (p.Gly27Glu) rs769331823 0.00006
NM_001377265.1(MAPT):c.2451C>T (p.Leu817=) rs200637464 0.00005
NM_001377265.1(MAPT):c.1453C>T (p.Leu485Phe) rs199759929 0.00004
NM_001377265.1(MAPT):c.1638G>A (p.Pro546=) rs201046056 0.00004
NM_001377265.1(MAPT):c.1733-12C>T rs373115116 0.00004
NM_001377265.1(MAPT):c.177G>A (p.Pro59=) rs370131551 0.00004
NM_001377265.1(MAPT):c.1881G>A (p.Ser627=) rs115142761 0.00004
NM_001377265.1(MAPT):c.220+2450A>G rs773274633 0.00004
NM_001377265.1(MAPT):c.220+2477C>G rs375470008 0.00004
NM_001377265.1(MAPT):c.2319C>T (p.Asn773=) rs746312281 0.00004
NM_001377265.1(MAPT):c.42C>T (p.His14=) rs759306195 0.00004
NM_001377265.1(MAPT):c.601C>T (p.Pro201Ser) rs776821664 0.00004
NM_001377265.1(MAPT):c.1238G>A (p.Arg413Gln) rs1261221296 0.00003
NM_001377265.1(MAPT):c.1377C>T (p.Asp459=) rs371173110 0.00003
NM_001377265.1(MAPT):c.1707C>T (p.Pro569=) rs750910229 0.00003
NM_001377265.1(MAPT):c.1767C>T (p.Tyr589=) rs750316359 0.00003
NM_001377265.1(MAPT):c.2034C>T (p.Asn678=) rs779043983 0.00003
NM_001377265.1(MAPT):c.2457G>A (p.Thr819=) rs369954009 0.00003
NM_001377265.1(MAPT):c.14G>A (p.Arg5His) rs63750959 0.00002
NM_001377265.1(MAPT):c.1632C>A (p.Ala544=) rs757701420 0.00002
NM_001377265.1(MAPT):c.1866T>C (p.Arg622=) rs778876874 0.00002
NM_001377265.1(MAPT):c.1884G>A (p.Pro628=) rs145897970 0.00002
NM_001377265.1(MAPT):c.2346G>A (p.Ala782=) rs771974951 0.00002
NM_001377265.1(MAPT):c.2418C>T (p.Thr806=) rs749816245 0.00002
NM_001377265.1(MAPT):c.36A>G (p.Glu12=) rs375852870 0.00002
NM_001377265.1(MAPT):c.769C>T (p.Arg257Cys) rs763093275 0.00002
NM_001377265.1(MAPT):c.969A>C (p.Thr323=) rs781607136 0.00002
NM_001377265.1(MAPT):c.1023C>G (p.Pro341=) rs1382449748 0.00001
NM_001377265.1(MAPT):c.1164G>T (p.Lys388Asn) rs759294645 0.00001
NM_001377265.1(MAPT):c.1327G>A (p.Val443Ile) rs774040384 0.00001
NM_001377265.1(MAPT):c.1347C>G (p.Leu449=) rs907474340 0.00001
NM_001377265.1(MAPT):c.1356C>A (p.Arg452=) rs776028517 0.00001
NM_001377265.1(MAPT):c.1407+18C>T rs957054703 0.00001
NM_001377265.1(MAPT):c.1417C>T (p.Arg473Cys) rs986393575 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.18G>A (p.Gln6=) rs769584478 0.00001
NM_001377265.1(MAPT):c.1956C>T (p.Ile652=) rs753776994 0.00001
NM_001377265.1(MAPT):c.2173+9G>C rs979650971 0.00001
NM_001377265.1(MAPT):c.220+2432G>A rs992572864 0.00001
NM_001377265.1(MAPT):c.220+2538C>G rs368845248 0.00001
NM_001377265.1(MAPT):c.2313C>T (p.Arg771=) rs373462041 0.00001
NM_001377265.1(MAPT):c.2364G>A (p.Ser788=) rs377720312 0.00001
NM_001377265.1(MAPT):c.261C>T (p.Asp87=) rs768654750 0.00001
NM_001377265.1(MAPT):c.690G>A (p.Gly230=) rs551008482 0.00001
NM_001377265.1(MAPT):c.963C>G (p.Pro321=) rs550945297 0.00001
NM_001377265.1(MAPT):c.973G>A (p.Ala325Thr) rs770014302 0.00001
NM_001377265.1(MAPT):c.*2616_*2618dup rs375986662
NM_001377265.1(MAPT):c.*65AAT[1] rs564954259
NM_001377265.1(MAPT):c.1115C>G (p.Ala372Gly) rs377402921
NM_001377265.1(MAPT):c.1146C>A (p.Ile382=) rs1598275540
NM_001377265.1(MAPT):c.1155C>T (p.Asn385=) rs745350248
NM_001377265.1(MAPT):c.1156G>A (p.Val386Met) rs747178896
NM_001377265.1(MAPT):c.1179G>A (p.Ser393=)
NM_001377265.1(MAPT):c.1179G>T (p.Ser393=)
NM_001377265.1(MAPT):c.1194A>G (p.Gly398=)
NM_001377265.1(MAPT):c.1218T>G (p.Pro406=)
NM_001377265.1(MAPT):c.1287C>T (p.Pro429=) rs772857557
NM_001377265.1(MAPT):c.133+7G>A
NM_001377265.1(MAPT):c.134-20G>C
NM_001377265.1(MAPT):c.1351+48_1351+56del rs138482356
NM_001377265.1(MAPT):c.1407+10C>T
NM_001377265.1(MAPT):c.1407+11G>A
NM_001377265.1(MAPT):c.150C>T (p.Thr50=)
NM_001377265.1(MAPT):c.153C>A (p.Pro51=)
NM_001377265.1(MAPT):c.1571C>G (p.Thr524Ser)
NM_001377265.1(MAPT):c.1606-18A>G
NM_001377265.1(MAPT):c.1606-19T>C
NM_001377265.1(MAPT):c.1629C>T (p.Ile543=) rs759212591
NM_001377265.1(MAPT):c.1677C>T (p.Asn559=)
NM_001377265.1(MAPT):c.1704G>T (p.Pro568=) rs1052551
NM_001377265.1(MAPT):c.1732+210dup rs1299153080
NM_001377265.1(MAPT):c.1732+2338C>T rs543103148
NM_001377265.1(MAPT):c.1732+2365C>A
NM_001377265.1(MAPT):c.1732+8_1732+10del rs745595533
NM_001377265.1(MAPT):c.1733-14T>C rs2145830502
NM_001377265.1(MAPT):c.1733-5C>T
NM_001377265.1(MAPT):c.1749A>C (p.Ser583=)
NM_001377265.1(MAPT):c.1752G>A (p.Gly584=)
NM_001377265.1(MAPT):c.177G>C (p.Pro59=) rs370131551
NM_001377265.1(MAPT):c.1794C>T (p.Pro598=)
NM_001377265.1(MAPT):c.1815G>A (p.Pro605=)
NM_001377265.1(MAPT):c.1830A>C (p.Pro610=)
NM_001377265.1(MAPT):c.1890C>T (p.Ser630=)
NM_001377265.1(MAPT):c.1971C>T (p.Asn657=)
NM_001377265.1(MAPT):c.1974G>A (p.Leu658=) rs373081497
NM_001377265.1(MAPT):c.1992C>T (p.Gly664=)
NM_001377265.1(MAPT):c.1995G>C (p.Gly665=)
NM_001377265.1(MAPT):c.1998+19G>A
NM_001377265.1(MAPT):c.1998+20C>T
NM_001377265.1(MAPT):c.1998+40C>T
NM_001377265.1(MAPT):c.1998+41G>A
NM_001377265.1(MAPT):c.1999-6C>A
NM_001377265.1(MAPT):c.2052C>T (p.Gly684=) rs1598380419
NM_001377265.1(MAPT):c.2091+11T>G
NM_001377265.1(MAPT):c.2091+17G>A
NM_001377265.1(MAPT):c.2092-18C>A
NM_001377265.1(MAPT):c.216G>A (p.Ala72=)
NM_001377265.1(MAPT):c.220+2477C>A
NM_001377265.1(MAPT):c.2205G>A (p.Lys735=)
NM_001377265.1(MAPT):c.2232G>C (p.Ser744=)
NM_001377265.1(MAPT):c.2268T>C (p.Pro756=)
NM_001377265.1(MAPT):c.2287-12C>T
NM_001377265.1(MAPT):c.2313C>A (p.Arg771=) rs373462041
NM_001377265.1(MAPT):c.2328C>T (p.Ala776=)
NM_001377265.1(MAPT):c.2436A>C (p.Val812=)
NM_001377265.1(MAPT):c.2445C>G (p.Pro815=)
NM_001377265.1(MAPT):c.39T>C (p.Asp13=)
NM_001377265.1(MAPT):c.444C>T (p.Thr148=)
NM_001377265.1(MAPT):c.58T>C (p.Leu20=)
NM_001377265.1(MAPT):c.63G>A (p.Gly21=)
NM_001377265.1(MAPT):c.756C>T (p.Asp252=) rs1358418932
NM_001377265.1(MAPT):c.757A>T (p.Thr253Ser) rs1598272763
NM_001377265.1(MAPT):c.889C>T (p.Arg297Cys) rs150983093
NM_001377265.1(MAPT):c.90C>A (p.Thr30=) rs1598169231
NM_001377265.1(MAPT):c.957G>A (p.Arg319=)

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