ClinVar Miner

List of variants in gene HNRNPU reported as likely benign for not provided

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Gene type:
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Total variants: 58
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HGVS dbSNP gnomAD frequency
NM_031844.3(HNRNPU):c.1017+117A>G rs141285794 0.00676
NM_031844.3(HNRNPU):c.2169C>T (p.Ala723=) rs11537737 0.00632
NM_031844.3(HNRNPU):c.1230+125del rs147249717 0.00558
NM_031844.3(HNRNPU):c.1495-132C>T rs111590102 0.00525
NM_031844.3(HNRNPU):c.141C>T (p.Ala47=) rs111518952 0.00501
NM_031844.3(HNRNPU):c.1017+50T>A rs116724293 0.00409
NM_031844.3(HNRNPU):c.1230+47T>C rs189965735 0.00363
NM_031844.3(HNRNPU):c.878-94G>C rs113453595 0.00286
NM_031844.3(HNRNPU):c.1743+8G>T rs75674611 0.00285
NM_031844.3(HNRNPU):c.1215G>A (p.Val405=) rs147232928 0.00161
NM_031844.3(HNRNPU):c.1744-47G>A rs377740635 0.00056
NM_031844.3(HNRNPU):c.2166A>C (p.Gly722=) rs140234240 0.00048
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.1744-37T>C rs202194880 0.00032
NM_031844.3(HNRNPU):c.2168-12C>G rs200427582 0.00025
NM_031844.3(HNRNPU):c.878-69G>A rs778202204 0.00017
NM_031844.3(HNRNPU):c.83A>G (p.Lys28Arg) rs200952460 0.00015
NM_031844.3(HNRNPU):c.1460G>C (p.Gly487Ala) rs199740131 0.00014
NM_031844.3(HNRNPU):c.621G>A (p.Gln207=) rs759528610 0.00013
NM_031844.3(HNRNPU):c.2227G>A (p.Gly743Ser) rs144984907 0.00011
NM_031844.3(HNRNPU):c.1274G>C (p.Gly425Ala) rs199596170 0.00008
NM_031844.3(HNRNPU):c.567C>T (p.Gly189=) rs756832741 0.00006
NM_031844.3(HNRNPU):c.282A>G (p.Glu94=) rs990170673 0.00005
NM_031844.3(HNRNPU):c.1434C>T (p.Asn478=) rs778730784 0.00004
NM_031844.3(HNRNPU):c.374A>C (p.Glu125Ala) rs199765762 0.00004
NM_031844.3(HNRNPU):c.2269C>T (p.Pro757Ser) rs921745963 0.00003
NM_031844.3(HNRNPU):c.680C>T (p.Ala227Val) rs755670533 0.00003
NM_031844.3(HNRNPU):c.875C>T (p.Thr292Ile) rs141449330 0.00003
NM_031844.3(HNRNPU):c.1996T>C (p.Leu666=) rs755861836 0.00002
NM_031844.3(HNRNPU):c.132C>T (p.Asp44=) rs1260101788 0.00001
NM_031844.3(HNRNPU):c.1439C>T (p.Pro480Leu) rs1171471843 0.00001
NM_031844.3(HNRNPU):c.1912+35T>A rs545348960 0.00001
NM_031844.3(HNRNPU):c.2193T>C (p.Asn731=) rs372228779 0.00001
NM_031844.3(HNRNPU):c.2226C>T (p.Gly742=) rs759916978 0.00001
NM_031844.3(HNRNPU):c.2285G>A (p.Arg762His) rs768453396 0.00001
NM_031844.3(HNRNPU):c.402C>T (p.Asp134=) rs1263252282 0.00001
NM_031844.3(HNRNPU):c.453C>T (p.Gly151=) rs757950940 0.00001
NM_031844.3(HNRNPU):c.489T>G (p.Pro163=) rs760562563 0.00001
NM_031844.3(HNRNPU):c.659G>T (p.Gly220Val) rs1463061163 0.00001
NM_031844.2(HNRNPU):c.2166_2167+1delAGG rs575582638
NM_031844.3(HNRNPU):c.-141C>T rs185164697
NM_031844.3(HNRNPU):c.1017+137TC[2] rs201625628
NM_031844.3(HNRNPU):c.1614+337A>G rs576831324
NM_031844.3(HNRNPU):c.1615-288_1615-285del rs200020281
NM_031844.3(HNRNPU):c.1743+5del rs2102985849
NM_031844.3(HNRNPU):c.264AGAGGA[1] (p.Glu93_Glu94del) rs770670938
NM_031844.3(HNRNPU):c.264AGAGGA[3] (p.Glu93_Glu94dup) rs770670938
NM_031844.3(HNRNPU):c.365AGG[3] (p.Glu125del) rs747108904
NM_031844.3(HNRNPU):c.373_374delinsCC (p.Glu125Pro)
NM_031844.3(HNRNPU):c.375G>C (p.Glu125Asp) rs752671029
NM_031844.3(HNRNPU):c.418G>A (p.Glu140Lys) rs1680927279
NM_031844.3(HNRNPU):c.495G>A (p.Pro165=) rs1230496425
NM_031844.3(HNRNPU):c.542A>C (p.Lys181Thr) rs747403316
NM_031844.3(HNRNPU):c.645G>A (p.Lys215=) rs772389068
NM_031844.3(HNRNPU):c.651AGGCGGCGG[1] (p.Gly221_Gly223del) rs757585114
NM_031844.3(HNRNPU):c.697G>A (p.Gly233Ser) rs771487560
NM_031844.3(HNRNPU):c.918C>T (p.Leu306=) rs1326720206

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