ClinVar Miner

List of variants in gene MLC1 reported as benign for brain disorder

Included ClinVar conditions (1840):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 64
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HGVS dbSNP gnomAD frequency
NM_015166.4(MLC1):c.321+50T>C rs79301 0.94928
NM_015166.4(MLC1):c.526-118C>T rs4838882 0.92209
NM_015166.4(MLC1):c.895-259G>A rs8142282 0.49774
NM_015166.4(MLC1):c.714+28G>A rs2038048 0.37853
NM_015166.4(MLC1):c.895-139G>A rs11568183 0.27262
NM_015166.4(MLC1):c.*1127C>T rs9628320 0.24216
NM_015166.4(MLC1):c.525+153G>A rs6010166 0.23729
NM_015166.4(MLC1):c.*48A>G rs137919 0.23521
NM_015166.4(MLC1):c.1059+16G>A rs5771338 0.17531
NM_015166.4(MLC1):c.894+194G>A rs2076127 0.16956
NM_015166.4(MLC1):c.*45A>G rs2072873 0.14823
NM_015166.4(MLC1):c.525+22G>A rs2072874 0.14143
NM_015166.4(MLC1):c.525+64G>A rs2076137 0.14127
NM_015166.3(MLC1):c.-561G>A rs4838883 0.13827
NM_015166.4(MLC1):c.*1764G>T rs41283489 0.13206
NM_015166.4(MLC1):c.771+175T>C rs2076132 0.11786
NM_015166.4(MLC1):c.771+160T>C rs2076133 0.11739
NM_015166.4(MLC1):c.771+59C>A rs2076135 0.11739
NM_015166.4(MLC1):c.771+61T>C rs2076134 0.11739
NM_015166.4(MLC1):c.772-35C>T rs11568179 0.11738
NM_015166.4(MLC1):c.894+52T>C rs5771349 0.11723
NM_015166.4(MLC1):c.894+199C>T rs5771142 0.11704
NM_015166.4(MLC1):c.895-9C>T rs11568185 0.11704
NM_015166.4(MLC1):c.895-23C>T rs11568184 0.11703
NM_015166.4(MLC1):c.*991T>G rs11704648 0.11696
NM_015166.4(MLC1):c.772-110A>G rs111258391 0.11687
NM_015166.4(MLC1):c.597A>G (p.Ser199=) rs6010164 0.11147
NM_015166.4(MLC1):c.594C>T (p.Tyr198=) rs6010165 0.11145
NM_015166.4(MLC1):c.978C>T (p.Cys326=) rs11568186 0.10918
NM_015166.4(MLC1):c.996T>C (p.Ser332=) rs11568187 0.10904
NM_015166.4(MLC1):c.*937C>T rs41283491 0.10778
NM_015166.4(MLC1):c.512G>T (p.Cys171Phe) rs6010260 0.10037
NM_015166.4(MLC1):c.*1836G>A rs11703598 0.09905
NM_015166.4(MLC1):c.895-261A>G rs8136173 0.09460
NM_015166.4(MLC1):c.1031A>G (p.Asn344Ser) rs11568188 0.09405
NM_015166.4(MLC1):c.771+158G>A rs35480507 0.08730
NM_015166.4(MLC1):c.1059+27A>G rs114282486 0.05667
NM_015166.4(MLC1):c.*1963C>G rs41283487 0.04214
NM_015166.4(MLC1):c.-59-17T>C rs9628323 0.03393
NM_015166.4(MLC1):c.*55C>T rs41283496 0.02067
NM_015166.4(MLC1):c.*1143C>T rs2294384 0.01944
NM_015166.4(MLC1):c.*970G>C rs117474715 0.01437
NM_015166.4(MLC1):c.*1773G>C rs80312581 0.01130
NM_015166.4(MLC1):c.*1334G>A rs2294382 0.01127
NM_015166.3(MLC1):c.-156C>T rs2076126 0.01015
NM_015166.4(MLC1):c.*339C>T rs115770001 0.00833
NM_015166.4(MLC1):c.*572C>T rs367816647 0.00818
NM_015166.4(MLC1):c.*1321A>G rs149073568 0.00778
NM_015166.4(MLC1):c.*12G>A rs142027672 0.00776
NM_015166.4(MLC1):c.932T>A (p.Val311Glu) rs141225099 0.00622
NM_015166.4(MLC1):c.279G>A (p.Ser93=) rs11568172 0.00422
NM_015166.4(MLC1):c.628G>A (p.Val210Ile) rs11568178 0.00110
NM_015166.4(MLC1):c.627C>T (p.Ala209=) rs138153307 0.00071
NM_015166.4(MLC1):c.601G>A (p.Val201Ile) rs147572634 0.00063
NM_015166.4(MLC1):c.1053T>C (p.Ala351=) rs11568190 0.00056
NM_015166.4(MLC1):c.*773G>A rs4838880 0.00039
NM_015166.4(MLC1):c.544G>A (p.Ala182Thr) rs537457768 0.00002
NM_015166.3(MLC1):c.-528dup rs137931
NM_015166.4(MLC1):c.*1623G>T rs35730155
NM_015166.4(MLC1):c.*661G>C rs376823805
NM_015166.4(MLC1):c.-59-14T>A rs141840641
NM_015166.4(MLC1):c.1052_1053insCGGGGAGGTGAGTGGCCTGTGGGGTGGGGGTGC (p.Val354_Ala355insSerGlyLeuTrpGlyGlyGlyAlaGlyGluVal) rs745656804
NM_015166.4(MLC1):c.654C>A (p.Asn218Lys) rs41302601
NM_015166.4(MLC1):c.772-80C>G rs75474964

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