ClinVar Miner

List of variants in gene NDRG1 reported as likely benign for not provided

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Gene type:
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Total variants: 44
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HGVS dbSNP gnomAD frequency
NM_006096.4(NDRG1):c.389+82G>T rs2233329 0.03173
NM_006096.4(NDRG1):c.*1622T>G rs7825439 0.02986
NM_006096.4(NDRG1):c.*264C>G rs73711834 0.02269
NM_006096.4(NDRG1):c.699-295A>G rs141156426 0.01373
NM_006096.4(NDRG1):c.-18-204G>A rs76043183 0.01294
NM_006096.4(NDRG1):c.808-288G>A rs73364559 0.01293
NM_006096.4(NDRG1):c.306C>T (p.Gly102=) rs2233322 0.01251
NM_006096.4(NDRG1):c.507G>A (p.Ala169=) rs2233331 0.01225
NM_006096.4(NDRG1):c.*69C>T rs114738844 0.01142
NM_006096.4(NDRG1):c.891+61G>A rs2233342 0.01073
NM_006096.4(NDRG1):c.100-40A>T rs143266148 0.00965
NM_006096.4(NDRG1):c.390-309T>C rs76311337 0.00924
NM_006096.4(NDRG1):c.594+46C>T rs76569722 0.00895
NM_006096.4(NDRG1):c.199A>G (p.Met67Val) rs2233319 0.00829
NM_006096.4(NDRG1):c.891+283G>A rs148462369 0.00798
NM_006096.4(NDRG1):c.699-238T>C rs114771875 0.00778
NM_006096.4(NDRG1):c.450+155G>A rs1060400 0.00526
NM_006096.4(NDRG1):c.944-175A>C rs527246669 0.00498
NM_006096.4(NDRG1):c.855+180A>G rs190091490 0.00479
NM_006096.4(NDRG1):c.879G>A (p.Pro293=) rs2233340 0.00458
NM_006096.4(NDRG1):c.450+213A>G rs116510858 0.00421
NM_006096.4(NDRG1):c.*25G>A rs149804385 0.00419
NM_006096.4(NDRG1):c.206-106A>C rs2233321 0.00345
NM_006096.4(NDRG1):c.205+53G>A rs2233320 0.00344
NM_006096.4(NDRG1):c.63+227A>G rs191635379 0.00309
NM_006096.4(NDRG1):c.-19+92G>A rs571319753 0.00291
NM_006096.4(NDRG1):c.331A>C (p.Met111Leu) rs2233328 0.00201
NM_006096.4(NDRG1):c.31G>A (p.Ala11Thr) rs145871479 0.00140
NM_006096.4(NDRG1):c.393G>A (p.Leu131=) rs149767690 0.00014
NM_006096.4(NDRG1):c.528C>T (p.Ala176=) rs191237702 0.00013
NM_006096.4(NDRG1):c.1053A>C (p.Arg351=) rs370153201 0.00010
NM_006096.4(NDRG1):c.1101C>T (p.Ser367=) rs201959970 0.00007
NM_006096.4(NDRG1):c.1155C>T (p.Ala385=) rs774605205 0.00004
NM_006096.4(NDRG1):c.808-6G>T rs779633074 0.00002
NM_006096.4(NDRG1):c.165C>T (p.Asn55=) rs368056707 0.00001
NM_006096.4(NDRG1):c.1077_1106dup (p.340TRSRSHTSEG[4]) rs1554747463
NM_006096.4(NDRG1):c.327-114del rs113590255
NM_006096.4(NDRG1):c.432C>T (p.Tyr144=) rs535684670
NM_006096.4(NDRG1):c.462T>G (p.Pro154=)
NM_006096.4(NDRG1):c.528C>G (p.Ala176=) rs191237702
NM_006096.4(NDRG1):c.64-20dup rs756038946
NM_006096.4(NDRG1):c.698+242C>T rs140613866
NM_006096.4(NDRG1):c.892-123C>A rs2233344
NM_006096.4(NDRG1):c.892-148_892-145del rs200823768

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