ClinVar Miner

List of variants in gene HNRNPU reported as uncertain significance for not provided

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Gene type:
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Total variants: 67
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HGVS dbSNP gnomAD frequency
NM_031844.3(HNRNPU):c.1259C>T (p.Ser420Leu) rs778010676 0.00003
NM_031844.3(HNRNPU):c.1214T>C (p.Val405Ala) rs936983140 0.00001
NM_031844.3(HNRNPU):c.1288G>A (p.Val430Ile) rs772732188 0.00001
NM_031844.3(HNRNPU):c.2333A>G (p.Asn778Ser) rs1680652178 0.00001
NM_031844.3(HNRNPU):c.2374A>C (p.Asn792His) rs770010858 0.00001
NM_031844.3(HNRNPU):c.386A>G (p.Glu129Gly) rs1435707336 0.00001
NM_031844.3(HNRNPU):c.533G>C (p.Gly178Ala) rs1345467904 0.00001
NM_031844.3(HNRNPU):c.*8A>C
NM_031844.3(HNRNPU):c.1018-13A>G rs1680766348
NM_031844.3(HNRNPU):c.1029G>C (p.Lys343Asn) rs1680765425
NM_031844.3(HNRNPU):c.1061T>C (p.Ile354Thr) rs2527882219
NM_031844.3(HNRNPU):c.1120GAA[2] (p.Glu376del) rs2102987167
NM_031844.3(HNRNPU):c.1145C>G (p.Ser382Cys)
NM_031844.3(HNRNPU):c.125T>C (p.Leu42Pro) rs1553284037
NM_031844.3(HNRNPU):c.1267A>C (p.Lys423Gln) rs2102986760
NM_031844.3(HNRNPU):c.127G>C (p.Asp43His)
NM_031844.3(HNRNPU):c.1340A>G (p.His447Arg)
NM_031844.3(HNRNPU):c.1368A>C (p.Glu456Asp) rs1558187433
NM_031844.3(HNRNPU):c.1387G>C (p.Glu463Gln) rs2527877146
NM_031844.3(HNRNPU):c.1411G>A (p.Glu471Lys) rs775402274
NM_031844.3(HNRNPU):c.1447G>A (p.Asp483Asn)
NM_031844.3(HNRNPU):c.1451G>A (p.Arg484Gln) rs2102986610
NM_031844.3(HNRNPU):c.1544C>T (p.Thr515Ile) rs1411908199
NM_031844.3(HNRNPU):c.158T>C (p.Met53Thr) rs2527896077
NM_031844.3(HNRNPU):c.1616T>A (p.Val539Glu)
NM_031844.3(HNRNPU):c.1617G>A (p.Val539=)
NM_031844.3(HNRNPU):c.1743G>A (p.Gln581=) rs1553282372
NM_031844.3(HNRNPU):c.1827A>C (p.Lys609Asn) rs1313822619
NM_031844.3(HNRNPU):c.1829A>G (p.Asp610Gly)
NM_031844.3(HNRNPU):c.1856A>G (p.Lys619Arg) rs1300093915
NM_031844.3(HNRNPU):c.1865_1867del (p.Glu622del) rs1553282322
NM_031844.3(HNRNPU):c.1881C>G (p.Asp627Glu) rs2527505510
NM_031844.3(HNRNPU):c.1895C>A (p.Ala632Glu) rs868735439
NM_031844.3(HNRNPU):c.2013A>C (p.Glu671Asp) rs373573514
NM_031844.3(HNRNPU):c.2053A>G (p.Thr685Ala) rs2102985384
NM_031844.3(HNRNPU):c.2119A>G (p.Arg707Gly) rs2102985342
NM_031844.3(HNRNPU):c.2168-8T>G rs1680658577
NM_031844.3(HNRNPU):c.2213A>G (p.Gln738Arg)
NM_031844.3(HNRNPU):c.2266G>C (p.Ala756Pro) rs1680654226
NM_031844.3(HNRNPU):c.226C>G (p.Gln76Glu) rs1221183673
NM_031844.3(HNRNPU):c.2351A>C (p.Gln784Pro) rs2102984930
NM_031844.3(HNRNPU):c.2366G>A (p.Arg789Gln) rs749543331
NM_031844.3(HNRNPU):c.2466A>T (p.Gln822His) rs1064796325
NM_031844.3(HNRNPU):c.250G>A (p.Glu84Lys)
NM_031844.3(HNRNPU):c.266_283dup (p.Glu89_Glu94dup) rs1558190683
NM_031844.3(HNRNPU):c.313G>C (p.Glu105Gln) rs2527895441
NM_031844.3(HNRNPU):c.374_375delinsCC (p.Glu125Ala) rs1680928684
NM_031844.3(HNRNPU):c.420A>C (p.Glu140Asp) rs1325726632
NM_031844.3(HNRNPU):c.436G>C (p.Gly146Arg) rs980758296
NM_031844.3(HNRNPU):c.450A>C (p.Glu150Asp) rs1461052775
NM_031844.3(HNRNPU):c.475G>C (p.Gly159Arg)
NM_031844.3(HNRNPU):c.479A>T (p.Glu160Val) rs2527894888
NM_031844.3(HNRNPU):c.503C>A (p.Thr168Lys)
NM_031844.3(HNRNPU):c.551C>G (p.Ala184Gly) rs1680922433
NM_031844.3(HNRNPU):c.651AGGCGGCGG[3] (p.Gly223_Arg224insGlyGlyGly)
NM_031844.3(HNRNPU):c.651_660del (p.Gly218fs) rs779453109
NM_031844.3(HNRNPU):c.661_669del (p.Gly221_Gly223del) rs2527893983
NM_031844.3(HNRNPU):c.669_691del (p.Arg224fs) rs754216321
NM_031844.3(HNRNPU):c.669_691dup (p.Gly231fs) rs754216321
NM_031844.3(HNRNPU):c.674C>G (p.Pro225Arg) rs1429007292
NM_031844.3(HNRNPU):c.691+1G>A rs1680915837
NM_031844.3(HNRNPU):c.691+1G>T
NM_031844.3(HNRNPU):c.767G>A (p.Gly256Glu)
NM_031844.3(HNRNPU):c.831AGA[2] (p.Glu279del) rs747301226
NM_031844.3(HNRNPU):c.871G>A (p.Asp291Asn)
NM_031844.3(HNRNPU):c.944G>A (p.Ser315Asn) rs1680795813
NM_031844.3(HNRNPU):c.994G>A (p.Gly332Ser) rs2527885175

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