List of variants in gene HNRNPU reported as benign

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 89

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HGVS	dbSNP	gnomAD frequency
NM_031844.3(HNRNPU):c.261G>A (p.Glu87=)	rs6675421	0.28406
NM_031844.3(HNRNPU):c.877+71T>A	rs12124462	0.27768
NM_031844.3(HNRNPU):c.1495-113G>C	rs9730334	0.21984
NM_031844.3(HNRNPU):c.1017+326C>T	rs12069105	0.21248
NM_031844.3(HNRNPU):c.1615-127A>G	rs1874393	0.15218
NM_031844.3(HNRNPU):c.877+70G>A	rs58736171	0.13080
NM_031844.3(HNRNPU):c.2352+102G>T	rs10927336	0.12879
NM_031844.3(HNRNPU):c.1017+272G>A	rs12079538	0.12422
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	0.02104
NM_031844.3(HNRNPU):c.803+11C>T	rs74152197	0.01701
NC_000001.11:g.244864715T>G	rs116239278	0.01649
NM_031844.3(HNRNPU):c.2169C>T (p.Ala723=)	rs11537737	0.00632
NM_031844.3(HNRNPU):c.141C>T (p.Ala47=)	rs111518952	0.00501
NM_031844.3(HNRNPU):c.1743+8G>T	rs75674611	0.00285
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.687G>A (p.Ala229=)	rs759259042	0.00046
NM_031844.3(HNRNPU):c.507G>A (p.Gln169=)	rs139561508	0.00045
NM_031844.3(HNRNPU):c.1251A>G (p.Val417=)	rs142767399	0.00041
NM_031844.3(HNRNPU):c.1460G>C (p.Gly487Ala)	rs199740131	0.00014
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.2424+16T>C	rs537512846	0.00006
NM_031844.3(HNRNPU):c.1794C>T (p.Gly598=)	rs369567187	0.00005
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.1081A>G (p.Ile361Val)	rs200962317	0.00003
NM_031844.3(HNRNPU):c.1086C>T (p.Gly362=)	rs556474465	0.00003
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.557A>T (p.Lys186Met)	rs372513810	0.00003
NM_031844.3(HNRNPU):c.1433A>G (p.Asn478Ser)	rs745596089	0.00002
NM_031844.3(HNRNPU):c.2204A>G (p.Asn735Ser)	rs1254900423	0.00002
NM_031844.3(HNRNPU):c.611G>C (p.Arg204Thr)	rs201849132	0.00002
NM_031844.3(HNRNPU):c.692-14C>T	rs201729220	0.00002
NM_031844.3(HNRNPU):c.1017+5A>G	rs1236536249	0.00001
NM_031844.3(HNRNPU):c.1369T>C (p.Phe457Leu)	rs2527877192	0.00001
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.1743+5G>A	rs1348831191	0.00001
NM_031844.3(HNRNPU):c.2009A>G (p.Lys670Arg)	rs937095421	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.2315A>G (p.Asn772Ser)	rs757462101	0.00001
NM_031844.3(HNRNPU):c.429T>C (p.Asp143=)	rs555895621	0.00001
NM_031844.3(HNRNPU):c.551C>T (p.Ala184Val)	rs1680922433	0.00001
NM_031844.3(HNRNPU):c.571A>G (p.Thr191Ala)	rs1680921585	0.00001
NM_031844.3(HNRNPU):c.607G>C (p.Ala203Pro)	rs773306715	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	rs765983864
NM_031844.3(HNRNPU):c.1391A>G (p.Lys464Arg)	rs1573331728
NM_031844.3(HNRNPU):c.1494+19_1494+21del	rs750413170
NM_031844.3(HNRNPU):c.1494+20_1494+21del	rs750413170
NM_031844.3(HNRNPU):c.1494+21del	rs750413170
NM_031844.3(HNRNPU):c.1495-10_1495-6del	rs759862936
NM_031844.3(HNRNPU):c.1614+5G>A	rs2102986339
NM_031844.3(HNRNPU):c.1744-11dup	rs770379796
NM_031844.3(HNRNPU):c.1744-4A>T	rs1242693487
NM_031844.3(HNRNPU):c.1913-3C>T	rs1424457995
NM_031844.3(HNRNPU):c.2167+39C>A	rs190132789
NM_031844.3(HNRNPU):c.2168-3dup	rs753707287
NM_031844.3(HNRNPU):c.2177A>G (p.Asn726Ser)	rs2527502885
NM_031844.3(HNRNPU):c.220C>T (p.Leu74Phe)
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.2353-114_2353-111del	rs59942516
NM_031844.3(HNRNPU):c.2464C>T (p.Gln822Ter)	rs542905297
NM_031844.3(HNRNPU):c.248A>G (p.Asp83Gly)
NM_031844.3(HNRNPU):c.249T>A (p.Asp83Glu)	rs1363572292
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)	rs570495195
NM_031844.3(HNRNPU):c.487C>T (p.Pro163Ser)	rs2527894856
NM_031844.3(HNRNPU):c.506A>G (p.Gln169Arg)	rs1680924291
NM_031844.3(HNRNPU):c.528G>C (p.Gln176His)	rs2527894655
NM_031844.3(HNRNPU):c.542A>C (p.Lys181Thr)	rs747403316
NM_031844.3(HNRNPU):c.542A>G (p.Lys181Arg)	rs747403316
NM_031844.3(HNRNPU):c.878-9T>C	rs573967558

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