ClinVar Miner

List of variants in gene MAPT reported as uncertain significance for Frontotemporal dementia

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Total variants: 33
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HGVS dbSNP
NM_001377265.1(MAPT):c.1008G>A (p.Ala336=) rs200385096
NM_001377265.1(MAPT):c.14G>A (p.Arg5His) rs63750959
NM_001377265.1(MAPT):c.1607G>A (p.Gly536Glu) rs116231676
NM_001377265.1(MAPT):c.1629C>G (p.Ile543Met) rs759212591
NM_001377265.1(MAPT):c.1630G>A (p.Ala544Thr) rs143624519
NM_001377265.1(MAPT):c.1703C>T (p.Pro568Leu) rs1273925499
NM_001377265.1(MAPT):c.1733-3del rs2074473044
NM_001377265.1(MAPT):c.1802G>A (p.Arg601His) rs115492908
NM_001377265.1(MAPT):c.1811C>A (p.Thr604Asn) rs763356972
NM_001377265.1(MAPT):c.1814C>T (p.Pro605Leu)
NM_001377265.1(MAPT):c.1831C>T (p.Pro611Ser) rs1598326219
NM_001377265.1(MAPT):c.1834A>C (p.Thr612Pro) rs1598326279
NM_001377265.1(MAPT):c.1891G>A (p.Ala631Thr) rs63750096
NM_001377265.1(MAPT):c.1982A>T (p.Gln661Leu) rs2074495003
NM_001377265.1(MAPT):c.1985C>T (p.Pro662Leu) rs1047467075
NM_001377265.1(MAPT):c.2014AAG[1] (p.Lys673del) rs63750688
NM_001377265.1(MAPT):c.2035G>A (p.Val679Ile) rs149280278
NM_001377265.1(MAPT):c.2173G>T (p.Gly725Ter) rs2076012350
NM_001377265.1(MAPT):c.2184G>C (p.Gln728His) rs1598408073
NM_001377265.1(MAPT):c.220+2490G>A rs371071165
NM_001377265.1(MAPT):c.220+2491C>T rs780582778
NM_001377265.1(MAPT):c.220+2503C>T rs138293088
NM_001377265.1(MAPT):c.2263G>A (p.Val755Ile) rs63750869
NM_001377265.1(MAPT):c.2286+6G>T rs2076343277
NM_001377265.1(MAPT):c.2313C>T (p.Arg771=) rs373462041
NM_001377265.1(MAPT):c.258A>C (p.Glu86Asp)
NM_001377265.1(MAPT):c.262G>A (p.Glu88Lys) rs373705830
NM_001377265.1(MAPT):c.47G>T (p.Gly16Val) rs755131800
NM_001377265.1(MAPT):c.62G>T (p.Gly21Val) rs781076528
NM_001377265.1(MAPT):c.630_640del (p.Phe211fs) rs768990943
NM_001377265.1(MAPT):c.841G>T (p.Ala281Ser) rs1321460540
NM_001377265.1(MAPT):c.889C>A (p.Arg297Ser) rs150983093
NM_001377265.1(MAPT):c.89C>T (p.Thr30Ile) rs374996228

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