ClinVar Miner

List of variants in gene HNRNPU reported as benign

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Gene type:
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Total variants: 73
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HGVS dbSNP gnomAD frequency
NM_031844.3(HNRNPU):c.261G>A (p.Glu87=) rs6675421 0.28876
NM_031844.3(HNRNPU):c.877+71T>A rs12124462 0.28294
NM_031844.3(HNRNPU):c.1495-113G>C rs9730334 0.21984
NM_031844.3(HNRNPU):c.1017+326C>T rs12069105 0.21897
NM_031844.3(HNRNPU):c.1615-127A>G rs1874393 0.15445
NM_031844.3(HNRNPU):c.877+70G>A rs58736171 0.13488
NM_031844.3(HNRNPU):c.2352+102G>T rs10927336 0.13048
NM_031844.3(HNRNPU):c.1017+272G>A rs12079538 0.12535
NM_031844.3(HNRNPU):c.1117+24T>G rs73128486 0.06036
NM_031844.3(HNRNPU):c.1615-209C>T rs76169958 0.05593
NM_031844.3(HNRNPU):c.1231-200T>A rs112642178 0.02318
NM_031844.3(HNRNPU):c.1117+153G>A rs79834162 0.02311
NM_031844.3(HNRNPU):c.2352+14A>T rs57080269 0.02263
NM_031844.3(HNRNPU):c.803+11C>T rs74152197 0.01825
NC_000001.11:g.244864715T>G rs116239278 0.01790
NM_031844.3(HNRNPU):c.2169C>T (p.Ala723=) rs11537737 0.00657
NM_031844.3(HNRNPU):c.141C>T (p.Ala47=) rs111518952 0.00536
NM_031844.3(HNRNPU):c.1743+8G>T rs75674611 0.00304
NM_031844.3(HNRNPU):c.1743+10A>C rs75053711 0.00248
NM_031844.3(HNRNPU):c.-41G>A rs376110167 0.00168
NM_031844.3(HNRNPU):c.1215G>A (p.Val405=) rs147232928 0.00161
NM_031844.3(HNRNPU):c.507G>A (p.Gln169=) rs139561508 0.00049
NM_031844.3(HNRNPU):c.1251A>G (p.Val417=) rs142767399 0.00045
NM_031844.3(HNRNPU):c.1208A>C (p.Asn403Thr) rs767181341 0.00006
NM_031844.3(HNRNPU):c.1319C>A (p.Ala440Asp) rs373039242 0.00006
NM_031844.3(HNRNPU):c.1460G>C (p.Gly487Ala) rs199740131 0.00005
NM_031844.3(HNRNPU):c.1081A>G (p.Ile361Val) rs200962317 0.00004
NM_031844.3(HNRNPU):c.1952A>C (p.Glu651Ala) rs202115297 0.00004
NM_031844.3(HNRNPU):c.374A>C (p.Glu125Ala) rs199765762 0.00004
NM_031844.3(HNRNPU):c.157A>G (p.Met53Val) rs770396451 0.00003
NM_031844.3(HNRNPU):c.1615-10T>C rs193281914 0.00003
NM_031844.3(HNRNPU):c.2204A>G (p.Asn735Ser) rs1254900423 0.00002
NM_031844.3(HNRNPU):c.2424+16T>C rs537512846 0.00002
NM_031844.3(HNRNPU):c.692-14C>T rs201729220 0.00002
NM_031844.3(HNRNPU):c.1405A>G (p.Ile469Val) rs370427995 0.00001
NM_031844.3(HNRNPU):c.1743+4C>T rs115917666 0.00001
NM_031844.3(HNRNPU):c.206G>C (p.Arg69Pro) rs754427497 0.00001
NM_031844.3(HNRNPU):c.2167+15A>C rs780932517 0.00001
NM_031844.3(HNRNPU):c.2168-6T>A rs1283465496 0.00001
NM_031844.3(HNRNPU):c.2193T>C (p.Asn731=) rs372228779 0.00001
NM_031844.3(HNRNPU):c.429T>C (p.Asp143=) rs555895621 0.00001
NM_031844.3(HNRNPU):c.877+47T>G rs372227800 0.00001
NM_031844.2(HNRNPU):c.2166_2167+1delAGG rs575582638
NM_031844.3(HNRNPU):c.1017+8C>T rs1553283026
NM_031844.3(HNRNPU):c.1118-30C>A rs145042684
NM_031844.3(HNRNPU):c.1231-12dup
NM_031844.3(HNRNPU):c.1391A>G (p.Lys464Arg) rs1573331728
NM_031844.3(HNRNPU):c.1494+19_1494+21del
NM_031844.3(HNRNPU):c.1494+20_1494+21del
NM_031844.3(HNRNPU):c.1494+21del rs750413170
NM_031844.3(HNRNPU):c.1495-10_1495-6del rs759862936
NM_031844.3(HNRNPU):c.1743+5G>A
NM_031844.3(HNRNPU):c.1744-11dup rs770379796
NM_031844.3(HNRNPU):c.2167+39C>A rs190132789
NM_031844.3(HNRNPU):c.2168-3dup
NM_031844.3(HNRNPU):c.2237G>T (p.Ser746Ile) rs1051595756
NM_031844.3(HNRNPU):c.2296T>G (p.Ser766Ala) rs746732226
NM_031844.3(HNRNPU):c.2315A>G (p.Asn772Ser)
NM_031844.3(HNRNPU):c.2353-114_2353-111del rs59942516
NM_031844.3(HNRNPU):c.2464C>T (p.Gln822Ter) rs542905297
NM_031844.3(HNRNPU):c.359C>G (p.Pro120Arg) rs1455165658
NM_031844.3(HNRNPU):c.374_375delinsCC (p.Glu125Ala) rs1680928684
NM_031844.3(HNRNPU):c.441C>G (p.Asp147Glu) rs539279281
NM_031844.3(HNRNPU):c.451G>A (p.Gly151Ser)
NM_031844.3(HNRNPU):c.487C>T (p.Pro163Ser)
NM_031844.3(HNRNPU):c.506A>G (p.Gln169Arg) rs1680924291
NM_031844.3(HNRNPU):c.528G>C (p.Gln176His)
NM_031844.3(HNRNPU):c.542A>C (p.Lys181Thr)
NM_031844.3(HNRNPU):c.542A>G (p.Lys181Arg) rs747403316
NM_031844.3(HNRNPU):c.557A>T (p.Lys186Met)
NM_031844.3(HNRNPU):c.607G>C (p.Ala203Pro)
NM_031844.3(HNRNPU):c.687G>A (p.Ala229=)
NM_031844.3(HNRNPU):c.878-9T>C rs573967558

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