ClinVar Miner

List of variants in gene MAPT reported as not provided

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Total variants: 61
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HGVS dbSNP
NM_001123066.3(MAPT):c.1321T>C (p.Tyr441His) rs2258689
NM_001123066.3(MAPT):c.1339T>C (p.Ser447Pro) rs10445337
NM_001123066.3(MAPT):c.1479G>A (p.Pro493=) rs1052551
NM_001123066.3(MAPT):c.1483G>A (p.Ala495Thr) rs63750612
NM_001123066.3(MAPT):c.1512T>C (p.Thr504=) rs62063845
NM_001123066.3(MAPT):c.1686A>G (p.Ala562=) rs1052553
NM_001123066.3(MAPT):c.1770T>C (p.Asn590=) rs17652121
NM_001123066.3(MAPT):c.1815G>A (p.Pro605=) rs11568305
NM_001123066.3(MAPT):c.605C>T (p.Pro202Leu) rs63750417
NM_001123066.3(MAPT):c.689A>G (p.Gln230Arg) rs63750072
NM_001123066.3(MAPT):c.853G>A (p.Asp285Asn) rs62063786
NM_001123066.3(MAPT):c.855C>T (p.Asp285=) rs63750222
NM_001123066.3(MAPT):c.866T>C (p.Val289Ala) rs62063787
NM_005910.5(MAPT):c.1087G>A (p.Val363Ile) rs63750869
NM_005910.5(MAPT):c.117G>A (p.Thr39=) rs63750529
NM_005910.5(MAPT):c.1216C>T (p.Arg406Trp) rs63750424
NM_005910.5(MAPT):c.715G>A (p.Ala239Thr) rs63750096
NM_005910.5(MAPT):c.837T>G (p.Asn279Lys) rs63750756
NM_005910.5(MAPT):c.841_843delAAG rs63750688
NM_005910.5(MAPT):c.902C>T (p.Pro301Leu) rs63751273
NM_005910.5(MAPT):c.903G>A (p.Pro301=) rs63751395
NM_005910.5(MAPT):c.915+16C>T rs63751011
NM_005910.5(MAPT):c.915+19C>G rs63750162
NM_005910.5(MAPT):c.915+25C>T rs63750117
NM_005910.5(MAPT):c.915+29G>A rs63751443
NM_005910.5(MAPT):c.915+3G>A rs63750013
NM_016835.4(MAPT):c.1107C>T (p.Ser369=) rs63750862
NM_016835.4(MAPT):c.14G>T (p.Arg5Leu) rs63750959
NM_016835.4(MAPT):c.1721A>C (p.Lys574Thr) rs63750129
NM_016835.4(MAPT):c.1729A>G (p.Ile577Val) rs63751249
NM_016835.4(MAPT):c.1747C>G (p.Leu583Val) rs63750349
NM_016835.4(MAPT):c.1766G>T (p.Gly589Val) rs63750376
NM_016835.4(MAPT):c.1774-10G>T rs63749974
NM_016835.4(MAPT):c.1803T>C (p.Leu601=) rs63751423
NM_016835.4(MAPT):c.1837A>C (p.Asn613His) rs63750416
NM_016835.4(MAPT):c.1838_1840delATA (p.Asn613del) rs63751392
NM_016835.4(MAPT):c.1839T>C (p.Asn613=) rs63750912
NM_016835.4(MAPT):c.1852C>T (p.Pro618Ser) rs63751438
NM_016835.4(MAPT):c.1859G>T (p.Gly620Val) rs63751391
NM_016835.4(MAPT):c.1865G>A (p.Ser622Asn) rs63751165
NM_016835.4(MAPT):c.1866+11T>C rs63751394
NM_016835.4(MAPT):c.1866+12C>T rs63750916
NM_016835.4(MAPT):c.1866+13A>G rs63750308
NM_016835.4(MAPT):c.1866+14C>T rs63750972
NM_016835.4(MAPT):c.1866T>C (p.Ser622=) rs63750568
NM_016835.4(MAPT):c.1895T>G (p.Leu632Arg) rs63749855
NM_016835.4(MAPT):c.1896G>A (p.Leu632=) rs63751231
NM_016835.4(MAPT):c.1901A>T (p.Lys634Met) rs63750092
NM_016835.4(MAPT):c.1910C>T (p.Ser637Phe) rs63750635
NM_016835.4(MAPT):c.1954G>A (p.Gly652Ser) rs63750095
NM_016835.4(MAPT):c.1955G>T (p.Gly652Val) rs63750905
NM_016835.4(MAPT):c.1958A>G (p.Gln653Arg) rs63750573
NM_016835.4(MAPT):c.1960G>A (p.Val654Met) rs63750570
NM_016835.4(MAPT):c.1976A>T (p.Glu659Val) rs63750711
NM_016835.4(MAPT):c.2006C>T (p.Ser669Leu) rs63750425
NM_016835.4(MAPT):c.2057A>T (p.Lys686Ile) rs63751264
NM_016835.4(MAPT):c.2116G>C (p.Gly706Arg) rs63750512
NM_016835.4(MAPT):c.2221C>A (p.Gln741Lys) rs63750191
NM_016835.4(MAPT):c.2231C>T (p.Thr744Met) rs63750991
NM_016835.4(MAPT):c.256G>A (p.Gly86Ser) rs63751135
NM_016835.4(MAPT):c.54C>T (p.Tyr18=) rs63750811

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