ClinVar Miner

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

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 71
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_001377265.1(MAPT):c.1505C>T (p.Ser502Phe) rs143956882 0.00169
NM_001377265.1(MAPT):c.1628T>C (p.Ile543Thr) rs114635790 0.00147
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.777C>T (p.Ala259=) rs370558032 0.00027
NM_001377265.1(MAPT):c.774C>T (p.His258=) rs761089103 0.00026
NM_001377265.1(MAPT):c.1567C>T (p.Arg523Ter) rs200099007 0.00011
NM_001377265.1(MAPT):c.678C>T (p.Ser226=) rs537438059 0.00011
NM_001377265.1(MAPT):c.1137C>T (p.His379=) rs142283842 0.00009
NM_001377265.1(MAPT):c.1938G>A (p.Lys646=) rs141636979 0.00009
NM_001377265.1(MAPT):c.1070C>T (p.Ser357Leu) rs199644237 0.00006
NM_001377265.1(MAPT):c.1623G>A (p.Thr541=) rs139748238 0.00006
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.601C>T (p.Pro201Ser) rs776821664 0.00004
NM_001377265.1(MAPT):c.1238G>A (p.Arg413Gln) rs1261221296 0.00003
NM_001377265.1(MAPT):c.1356C>A (p.Arg452=) rs776028517 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.2271C>T (p.Gly757=) rs148501218 0.00003
NM_001377265.1(MAPT):c.1884G>A (p.Pro628=) rs145897970 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.1417C>T (p.Arg473Cys) rs986393575 0.00001
NM_001377265.1(MAPT):c.1776C>T (p.Pro592=) rs201057449 0.00001
NM_001377265.1(MAPT):c.2173+9G>C rs979650971 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.973G>A (p.Ala325Thr) rs770014302 0.00001
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.1287C>T (p.Pro429=) rs772857557
NM_001377265.1(MAPT):c.1407+18C>T
NM_001377265.1(MAPT):c.1629C>T (p.Ile543=)
NM_001377265.1(MAPT):c.1704G>T (p.Pro568=)
NM_001377265.1(MAPT):c.1732+2338C>T rs543103148
NM_001377265.1(MAPT):c.1732+8_1732+10del
NM_001377265.1(MAPT):c.1733-12C>T
NM_001377265.1(MAPT):c.1733-14T>C
NM_001377265.1(MAPT):c.1767C>T (p.Tyr589=)
NM_001377265.1(MAPT):c.177G>A (p.Pro59=)
NM_001377265.1(MAPT):c.177G>C (p.Pro59=)
NM_001377265.1(MAPT):c.1854G>A (p.Val618=)
NM_001377265.1(MAPT):c.1866T>C (p.Arg622=)
NM_001377265.1(MAPT):c.1881G>A (p.Ser627=)
NM_001377265.1(MAPT):c.18G>A (p.Gln6=)
NM_001377265.1(MAPT):c.1956C>T (p.Ile652=)
NM_001377265.1(MAPT):c.1998+15C>T
NM_001377265.1(MAPT):c.2034C>T (p.Asn678=)
NM_001377265.1(MAPT):c.2052C>T (p.Gly684=) rs1598380419
NM_001377265.1(MAPT):c.2074G>A (p.Val692Ile)
NM_001377265.1(MAPT):c.220+2480G>A
NM_001377265.1(MAPT):c.2262C>T (p.His754=)
NM_001377265.1(MAPT):c.2313C>A (p.Arg771=)
NM_001377265.1(MAPT):c.2346G>A (p.Ala782=)
NM_001377265.1(MAPT):c.2418C>T (p.Thr806=)
NM_001377265.1(MAPT):c.2451C>T (p.Leu817=)
NM_001377265.1(MAPT):c.273T>C (p.Gly91=)
NM_001377265.1(MAPT):c.36A>G (p.Glu12=)
NM_001377265.1(MAPT):c.42C>T (p.His14=)
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

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.