ClinVar Miner

List of variants in gene combination KANSL1, MAPT reported as likely benign for MAPT-Related Spectrum Disorders

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Total variants: 21
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HGVS dbSNP
NM_001193466.2(KANSL1):c.*1027C>G rs11870461
NM_001193466.2(KANSL1):c.*1028T>C rs375427074
NM_001193466.2(KANSL1):c.*1196T>G rs137970866
NM_001193466.2(KANSL1):c.*217C>T rs140200874
NM_001193466.2(KANSL1):c.*34_*37del rs373668834
NM_001193466.2(KANSL1):c.*388G>T rs367998611
NM_001193466.2(KANSL1):c.*626T>C rs533537317
NM_005910.5(MAPT):c.*1039C>T rs568260584
NM_005910.5(MAPT):c.*1404T>C rs530779128
NM_005910.5(MAPT):c.*1465C>T rs189665411
NM_005910.5(MAPT):c.*1670C>T rs535931288
NM_005910.5(MAPT):c.*1721C>T rs186042163
NM_005910.5(MAPT):c.*2167G>A rs16940802
NM_005910.5(MAPT):c.*2956T>C rs181844055
NM_005910.5(MAPT):c.*2991C>T rs141337757
NM_005910.5(MAPT):c.*3133A>G rs191084195
NM_005910.5(MAPT):c.*3377G>C rs540687358
NM_005910.5(MAPT):c.*3435T>C rs186977284
NM_005910.5(MAPT):c.*3570T>C rs567899904
NM_005910.5(MAPT):c.*3810G>A rs140613804
NM_005910.5(MAPT):c.*4154T>C rs377535401

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