ClinVar Miner

List of variants in gene MAPT reported as likely benign by Invitae

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Total variants: 48
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HGVS dbSNP
NM_001377265.1(MAPT):c.1023C>G (p.Pro341=) rs1382449748
NM_001377265.1(MAPT):c.1070C>T (p.Ser357Leu) rs199644237
NM_001377265.1(MAPT):c.1115C>G (p.Ala372Gly) rs377402921
NM_001377265.1(MAPT):c.1137C>T (p.His379=) rs142283842
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.1164G>T (p.Lys388Asn) rs759294645
NM_001377265.1(MAPT):c.120C>T (p.Asp40=) rs191362093
NM_001377265.1(MAPT):c.1238G>A (p.Arg413Gln) rs1261221296
NM_001377265.1(MAPT):c.1287C>T (p.Pro429=) rs772857557
NM_001377265.1(MAPT):c.1327G>A (p.Val443Ile) rs774040384
NM_001377265.1(MAPT):c.1347C>G (p.Leu449=) rs907474340
NM_001377265.1(MAPT):c.1356C>A (p.Arg452=) rs776028517
NM_001377265.1(MAPT):c.1377C>T (p.Asp459=) rs371173110
NM_001377265.1(MAPT):c.1417C>T (p.Arg473Cys) rs986393575
NM_001377265.1(MAPT):c.1453C>T (p.Leu485Phe) rs199759929
NM_001377265.1(MAPT):c.1505C>T (p.Ser502Phe) rs143956882
NM_001377265.1(MAPT):c.1567C>T (p.Arg523Ter) rs200099007
NM_001377265.1(MAPT):c.1623G>A (p.Thr541=) rs139748238
NM_001377265.1(MAPT):c.1628T>C (p.Ile543Thr) rs114635790
NM_001377265.1(MAPT):c.1638G>A (p.Pro546=) rs201046056
NM_001377265.1(MAPT):c.1707C>T (p.Pro569=) rs750910229
NM_001377265.1(MAPT):c.1732+2338C>T rs543103148
NM_001377265.1(MAPT):c.1776C>T (p.Pro592=) rs201057449
NM_001377265.1(MAPT):c.177G>C (p.Pro59=)
NM_001377265.1(MAPT):c.1881G>A (p.Ser627=)
NM_001377265.1(MAPT):c.1938G>A (p.Lys646=) rs141636979
NM_001377265.1(MAPT):c.1956C>T (p.Ile652=)
NM_001377265.1(MAPT):c.2034C>T (p.Asn678=)
NM_001377265.1(MAPT):c.2052C>T (p.Gly684=) rs1598380419
NM_001377265.1(MAPT):c.2271C>T (p.Gly757=) rs148501218
NM_001377265.1(MAPT):c.2313C>A (p.Arg771=)
NM_001377265.1(MAPT):c.2418C>T (p.Thr806=)
NM_001377265.1(MAPT):c.261C>T (p.Asp87=) rs768654750
NM_001377265.1(MAPT):c.50C>T (p.Thr17Met) rs144611688
NM_001377265.1(MAPT):c.601C>T (p.Pro201Ser) rs776821664
NM_001377265.1(MAPT):c.678C>T (p.Ser226=) rs537438059
NM_001377265.1(MAPT):c.690G>A (p.Gly230=) rs551008482
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.769C>T (p.Arg257Cys) rs763093275
NM_001377265.1(MAPT):c.774C>T (p.His258=) rs761089103
NM_001377265.1(MAPT):c.777C>T (p.Ala259=) rs370558032
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.969A>C (p.Thr323=) rs781607136
NM_001377265.1(MAPT):c.973G>A (p.Ala325Thr) rs770014302

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