ClinVar Miner

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

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Gene type:
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Total variants: 58
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HGVS dbSNP
NM_001377265.1(MAPT):c.-17-215C>T
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.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.1178C>T (p.Ser393Leu) rs73314997
NM_001377265.1(MAPT):c.117G>A (p.Thr39=) rs63750529
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.1326C>T (p.Pro442=)
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.1351+21C>T
NM_001377265.1(MAPT):c.1351+48_1351+56del
NM_001377265.1(MAPT):c.1351+52C>T
NM_001377265.1(MAPT):c.1352-103C>T
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.1567C>T (p.Arg523Ter) rs200099007
NM_001377265.1(MAPT):c.1676A>G (p.Asn559Ser) rs150420625
NM_001377265.1(MAPT):c.1732+195C>A
NM_001377265.1(MAPT):c.1732+210dup
NM_001377265.1(MAPT):c.1732+2338C>T rs543103148
NM_001377265.1(MAPT):c.1733-31T>C
NM_001377265.1(MAPT):c.1938G>A (p.Lys646=) rs141636979
NM_001377265.1(MAPT):c.1998+147C>T
NM_001377265.1(MAPT):c.2052C>T (p.Gly684=) rs1598380419
NM_001377265.1(MAPT):c.2091+29G>A rs63751443
NM_001377265.1(MAPT):c.2092-192C>T
NM_001377265.1(MAPT):c.220+2202G>A
NM_001377265.1(MAPT):c.220+2432G>A
NM_001377265.1(MAPT):c.220+2477C>G
NM_001377265.1(MAPT):c.220+2538C>G rs368845248
NM_001377265.1(MAPT):c.2286+109G>C
NM_001377265.1(MAPT):c.2349G>A (p.Glu783=) rs142776675
NM_001377265.1(MAPT):c.261C>T (p.Asp87=) rs768654750
NM_001377265.1(MAPT):c.427G>T (p.Ala143Ser)
NM_001377265.1(MAPT):c.464G>A (p.Arg155His)
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.862G>A (p.Gly288Arg) rs76375268
NM_001377265.1(MAPT):c.889C>A (p.Arg297Ser) rs150983093
NM_001377265.1(MAPT):c.889C>T (p.Arg297Cys) rs150983093
NM_001377265.1(MAPT):c.896T>G (p.Val299Gly) rs141120474
NM_001377265.1(MAPT):c.90C>A (p.Thr30=) rs1598169231
NM_001377265.1(MAPT):c.921C>G (p.Ser307=)
NM_001377265.1(MAPT):c.963C>G (p.Pro321=) rs550945297
NM_001377265.1(MAPT):c.969A>C (p.Thr323=) rs781607136

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