ClinVar Miner

List of variants in gene combination KANSL1, MAPT

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Total variants: 61
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HGVS dbSNP
NM_001123066.3(MAPT):c.*1145_*1146insT rs1491446284
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.*1235dup rs140510364
NM_001193466.2(KANSL1):c.*1328del rs71665335
NM_001193466.2(KANSL1):c.*1354del rs67641084
NM_001193466.2(KANSL1):c.*1520del rs67801660
NM_001193466.2(KANSL1):c.*217C>T rs140200874
NM_001193466.2(KANSL1):c.*34_*37del rs373668834
NM_001193466.2(KANSL1):c.*359_*360insAGAGGGC rs113448888
NM_001193466.2(KANSL1):c.*388G>T rs367998611
NM_001193466.2(KANSL1):c.*487C>T rs17652961
NM_001193466.2(KANSL1):c.*626T>C rs533537317
NM_001193466.2(KANSL1):c.*640T>C rs17574361
NM_001193466.2(KANSL1):c.*742G>A rs7350928
NM_001193466.2(KANSL1):c.*885del rs5820607
NM_001193466.2(KANSL1):c.2742C>T (p.Asp914=) rs35833914
NM_001193466.2(KANSL1):c.2751C>T (p.Phe917=) rs36076725
NM_001193466.2(KANSL1):c.3029C>T (p.Pro1010Leu) rs7220988
NM_001193466.2(KANSL1):c.3254T>C (p.Ile1085Thr) rs34579536
NM_001377265.1(MAPT):c.*3216C>A
NM_001377265.1(MAPT):c.*3371G>A
NM_001377265.1(MAPT):c.*3571C>A
NM_001377265.1(MAPT):c.*3589G>A
NM_001377265.1(MAPT):c.*3951G>A
NM_001377265.1(MAPT):c.*4004C>T
NM_001377265.1(MAPT):c.*4071G>A
NM_005910.5(MAPT):c.*1039C>T rs568260584
NM_005910.5(MAPT):c.*1047C>T rs113815715
NM_005910.5(MAPT):c.*1067T>C rs1052587
NM_005910.5(MAPT):c.*1101A>G rs1052590
NM_005910.5(MAPT):c.*1152G>C rs1052594
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.*1759T>C rs7687
NM_005910.5(MAPT):c.*2079C>T rs17652748
NM_005910.5(MAPT):c.*2167G>A rs16940802
NM_005910.5(MAPT):c.*2269G>T rs73317039
NM_005910.5(MAPT):c.*2806A>C rs2158257
NM_005910.5(MAPT):c.*2810G>A rs2158256
NM_005910.5(MAPT):c.*2956T>C rs181844055
NM_005910.5(MAPT):c.*2972T>C rs17574228
NM_005910.5(MAPT):c.*2991C>T rs141337757
NM_005910.5(MAPT):c.*3079=
NM_005910.5(MAPT):c.*3133A>G rs191084195
NM_005910.5(MAPT):c.*3319T>C rs763646469
NM_005910.5(MAPT):c.*3377G>C rs540687358
NM_005910.5(MAPT):c.*3381G>C rs886053054
NM_005910.5(MAPT):c.*3435T>C rs186977284
NM_005910.5(MAPT):c.*3570T>C rs567899904
NM_005910.5(MAPT):c.*3765G>A rs754252154
NM_005910.5(MAPT):c.*3810G>A rs140613804
NM_005910.5(MAPT):c.*3817G>A rs886053055
NM_005910.5(MAPT):c.*3848A>G rs114213384
NM_005910.5(MAPT):c.*3858A>G rs7521
NM_005910.5(MAPT):c.*3872_*3874dup rs886053056
NM_005910.5(MAPT):c.*4154T>C rs377535401
NM_016834.5(MAPT):c.*3358_*3360TGT[1] rs886053053

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