ClinVar Miner

List of variants in gene MOCS1 reported as uncertain significance for Molybdenum cofactor deficiency, complementation group A

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Total variants: 79
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HGVS dbSNP
NM_001358530.2(MOCS1):c.*1003G>A rs374341048
NM_001358530.2(MOCS1):c.*1046A>T
NM_001358530.2(MOCS1):c.*1063T>A rs886061383
NM_001358530.2(MOCS1):c.*1067A>C rs754337805
NM_001358530.2(MOCS1):c.*1117A>C rs886061381
NM_001358530.2(MOCS1):c.*1305C>T rs7744483
NM_001358530.2(MOCS1):c.*1307A>G
NM_001358530.2(MOCS1):c.*1341T>A
NM_001358530.2(MOCS1):c.*135T>G rs370974142
NM_001358530.2(MOCS1):c.*142C>G
NM_001358530.2(MOCS1):c.*1436C>T rs886061380
NM_001358530.2(MOCS1):c.*1445C>T rs575187638
NM_001358530.2(MOCS1):c.*282T>C
NM_001358530.2(MOCS1):c.*2A>G rs767003803
NM_001358530.2(MOCS1):c.*326C>T
NM_001358530.2(MOCS1):c.*400C>T rs764443066
NM_001358530.2(MOCS1):c.*477C>T rs184315150
NM_001358530.2(MOCS1):c.*523T>C
NM_001358530.2(MOCS1):c.*633C>T
NM_001358530.2(MOCS1):c.*638C>G rs886061386
NM_001358530.2(MOCS1):c.*659A>G
NM_001358530.2(MOCS1):c.*664T>C rs148100667
NM_001358530.2(MOCS1):c.*739C>T rs886061385
NM_001358530.2(MOCS1):c.*756A>C
NM_001358530.2(MOCS1):c.*762G>A rs115429345
NM_001358530.2(MOCS1):c.*76T>C
NM_001358530.2(MOCS1):c.*803C>T
NM_001358530.2(MOCS1):c.*84A>G rs752606397
NM_001358530.2(MOCS1):c.*888C>T
NM_001358530.2(MOCS1):c.1015C>T (p.Arg339Trp) rs148579886
NM_001358530.2(MOCS1):c.1016G>A (p.Arg339Gln) rs142478972
NM_001358530.2(MOCS1):c.1028G>A (p.Arg343Gln) rs781187745
NM_001358530.2(MOCS1):c.1064T>C (p.Ile355Thr) rs143912353
NM_001358530.2(MOCS1):c.1098T>G (p.His366Gln)
NM_001358530.2(MOCS1):c.1102+1_1102+2del rs1562086288
NM_001358530.2(MOCS1):c.1106T>A (p.Met369Lys)
NM_001358530.2(MOCS1):c.1132C>G (p.Arg378Gly)
NM_001358530.2(MOCS1):c.1150G>A (p.Glu384Lys) rs751603831
NM_001358530.2(MOCS1):c.1211C>T (p.Pro404Leu) rs570962724
NM_001358530.2(MOCS1):c.1226G>A (p.Gly409Asp)
NM_001358530.2(MOCS1):c.124-167C>T
NM_001358530.2(MOCS1):c.124-176A>T
NM_001358530.2(MOCS1):c.124-69G>A rs45487695
NM_001358530.2(MOCS1):c.1282A>G (p.Arg428Gly) rs886061389
NM_001358530.2(MOCS1):c.1315C>T (p.Arg439Trp)
NM_001358530.2(MOCS1):c.1362C>T (p.Asp454=)
NM_001358530.2(MOCS1):c.1367A>T (p.Asp456Val) rs143730711
NM_001358530.2(MOCS1):c.1400G>A (p.Trp467Ter)
NM_001358530.2(MOCS1):c.1413C>T (p.Ala471=) rs745789021
NM_001358530.2(MOCS1):c.152G>T (p.Arg51Leu) rs754387991
NM_001358530.2(MOCS1):c.156G>C (p.Glu52Asp) rs766904353
NM_001358530.2(MOCS1):c.1628C>A (p.Ala543Glu) rs886061388
NM_001358530.2(MOCS1):c.162G>A (p.Ala54=) rs200316862
NM_001358530.2(MOCS1):c.1668C>T (p.His556=)
NM_001358530.2(MOCS1):c.1714C>T (p.Arg572Cys)
NM_001358530.2(MOCS1):c.175G>T (p.Ala59Ser) rs770756364
NM_001358530.2(MOCS1):c.1788T>G (p.Ser596=) rs200764011
NM_001358530.2(MOCS1):c.1822T>C (p.Cys608Arg)
NM_001358530.2(MOCS1):c.264G>A (p.Met88Ile) rs144238782
NM_001358530.2(MOCS1):c.282G>A (p.Pro94=)
NM_001358530.2(MOCS1):c.301C>T (p.Leu101=)
NM_001358530.2(MOCS1):c.339C>T (p.Leu113=)
NM_001358530.2(MOCS1):c.358G>C (p.Asp120His) rs368420298
NM_001358530.2(MOCS1):c.394C>T (p.Arg132Trp) rs377167949
NM_001358530.2(MOCS1):c.398C>T (p.Pro133Leu)
NM_001358530.2(MOCS1):c.544C>A (p.Leu182Met)
NM_001358530.2(MOCS1):c.583+12T>C
NM_001358530.2(MOCS1):c.583+7G>A
NM_001358530.2(MOCS1):c.616G>A (p.Ala206Thr)
NM_001358530.2(MOCS1):c.644A>G (p.Lys215Arg) rs887485143
NM_001358530.2(MOCS1):c.707C>T (p.Thr236Ile)
NM_001358530.2(MOCS1):c.719C>T (p.Pro240Leu)
NM_001358530.2(MOCS1):c.729G>A (p.Val243=) rs886061390
NM_001358530.2(MOCS1):c.758-9C>T rs368402544
NM_001358530.2(MOCS1):c.77C>T (p.Pro26Leu)
NM_001358530.2(MOCS1):c.814C>T (p.Arg272Trp) rs146944225
NM_001358530.2(MOCS1):c.853G>A (p.Glu285Lys) rs140243105
NM_001358530.2(MOCS1):c.868A>C (p.Lys290Gln)
NM_001358530.2(MOCS1):c.981+12C>T rs377628500

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