ClinVar Miner

List of variants in gene combination KANSL1, MAPT reported by Illumina Laboratory Services, Illumina

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Gene type:
ClinVar version:
Total variants: 47
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HGVS dbSNP gnomAD frequency
NM_001377265.1(MAPT):c.*1145_*1146insT rs1491446284 0.40313
NM_015443.4(KANSL1):c.3029C>T (p.Pro1010Leu) rs7220988 0.34127
NM_001377265.1(MAPT):c.*1101A>G rs1052590 0.14499
NM_001377265.1(MAPT):c.*1759T>C rs7687 0.14487
NM_015443.4(KANSL1):c.*487C>T rs17652961 0.14478
NM_001377265.1(MAPT):c.*2806A>C rs2158257 0.14473
NM_001377265.1(MAPT):c.*1067T>C rs1052587 0.14468
NM_015443.4(KANSL1):c.3254T>C (p.Ile1085Thr) rs34579536 0.14468
NM_001377265.1(MAPT):c.*2972T>C rs17574228 0.14466
NM_015443.4(KANSL1):c.*640T>C rs17574361 0.14457
NM_001377265.1(MAPT):c.*2079C>T rs17652748 0.14441
NM_015443.4(KANSL1):c.2742C>T (p.Asp914=) rs35833914 0.14434
NM_015443.4(KANSL1):c.2751C>T (p.Phe917=) rs36076725 0.14426
NM_015443.4(KANSL1):c.*742G>A rs7350928 0.12614
NM_001377265.1(MAPT):c.*1152G>C rs1052594 0.12578
NM_001377265.1(MAPT):c.*2269G>T rs73317039 0.03265
NM_001377265.1(MAPT):c.*3848A>G rs114213384 0.03189
NM_001377265.1(MAPT):c.*1047C>T rs113815715 0.02477
NM_001377265.1(MAPT):c.*2810G>A rs2158256 0.02237
NM_001377265.1(MAPT):c.*2167G>A rs16940802 0.01564
NM_001377265.1(MAPT):c.*2991C>T rs141337757 0.01116
NM_001377265.1(MAPT):c.*3435T>C rs186977284 0.00544
NM_001377265.1(MAPT):c.*2956T>C rs181844055 0.00514
NM_015443.4(KANSL1):c.*1196T>G rs137970866 0.00488
NM_015443.4(KANSL1):c.*1027C>G rs11870461 0.00390
NM_015443.4(KANSL1):c.*34_*37del rs373668834 0.00257
NM_001377265.1(MAPT):c.*3377G>C rs540687358 0.00235
NM_001377265.1(MAPT):c.*1721C>T rs186042163 0.00190
NM_015443.4(KANSL1):c.*217C>T rs140200874 0.00136
NM_001377265.1(MAPT):c.*3570T>C rs567899904 0.00098
NM_001377265.1(MAPT):c.*1465C>T rs189665411 0.00039
NM_015443.4(KANSL1):c.*626T>C rs533537317 0.00022
NM_001377265.1(MAPT):c.*3810G>A rs140613804 0.00007
NM_001377265.1(MAPT):c.*3133A>G rs191084195 0.00002
NM_001377265.1(MAPT):c.*1670C>T rs535931288 0.00001
NM_001377265.1(MAPT):c.*4154T>C rs377535401 0.00001
NM_001377265.1(MAPT):c.*1039C>T rs568260584
NM_001377265.1(MAPT):c.*1404T>C rs530779128
NM_001377265.1(MAPT):c.*3078=
NM_015443.4(KANSL1):c.*1028T>C rs375427074
NM_015443.4(KANSL1):c.*1235dup rs140510364
NM_015443.4(KANSL1):c.*1328del rs71665335
NM_015443.4(KANSL1):c.*1354del rs67641084
NM_015443.4(KANSL1):c.*1520del rs67801660
NM_015443.4(KANSL1):c.*359_*360insAGAGGGC rs113448888
NM_015443.4(KANSL1):c.*388G>T rs367998611
NM_015443.4(KANSL1):c.*885del rs5820607

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