ClinVar Miner

List of variants in gene CDKN1B reported as benign

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Total variants: 56
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HGVS dbSNP gnomAD frequency
NM_004064.5(CDKN1B):c.-79T>C rs34330 0.69820
NM_004064.5(CDKN1B):c.*956C>A rs7330 0.55098
NM_004064.5(CDKN1B):c.*9-222T>C rs34327 0.49862
NM_004064.5(CDKN1B):c.326T>G (p.Val109Gly) rs2066827 0.36014
NM_004064.5(CDKN1B):c.*181T>C rs4251696 0.01260
NM_004064.5(CDKN1B):c.*501G>A rs4251697 0.00638
NM_004064.5(CDKN1B):c.-266C>G rs3093728 0.00372
NM_004064.5(CDKN1B):c.426G>A (p.Thr142=) rs149775942 0.00366
NM_004064.5(CDKN1B):c.577C>T (p.Leu193Phe) rs73281150 0.00338
NM_004064.5(CDKN1B):c.*833T>A rs141549130 0.00298
NM_004064.5(CDKN1B):c.-126C>T rs549943001 0.00118
NM_004064.5(CDKN1B):c.475+10C>T rs36101844 0.00096
NM_004064.5(CDKN1B):c.165G>A (p.Ala55=) rs16908375 0.00068
NM_004064.5(CDKN1B):c.543C>G (p.Ala181=) rs140177202 0.00064
NM_004064.5(CDKN1B):c.356T>C (p.Ile119Thr) rs142833529 0.00057
NM_004064.5(CDKN1B):c.518A>G (p.Asn173Ser) rs141509450 0.00042
NM_004064.5(CDKN1B):c.155T>G (p.Met52Arg) rs543122580 0.00037
NM_004064.5(CDKN1B):c.114C>T (p.His38=) rs141178987 0.00031
NM_004064.5(CDKN1B):c.476-5C>T rs370509436 0.00031
NM_004064.5(CDKN1B):c.476-6G>A rs376695255 0.00031
NM_004064.5(CDKN1B):c.*9-9C>G rs755164166 0.00023
NM_004064.5(CDKN1B):c.-80C>T rs551236750 0.00021
NM_004064.5(CDKN1B):c.407A>G (p.Asp136Gly) rs546234840 0.00020
NM_004064.5(CDKN1B):c.373T>A (p.Ser125Thr) rs765681672 0.00017
NM_004064.5(CDKN1B):c.482C>G (p.Ser161Cys) rs373917399 0.00014
NM_004064.5(CDKN1B):c.281C>T (p.Pro94Leu) rs757917082 0.00011
NM_004064.5(CDKN1B):c.-10C>T rs374913823 0.00009
NM_004064.5(CDKN1B):c.125C>T (p.Thr42Ile) rs200422211 0.00009
NM_004064.5(CDKN1B):c.54C>T (p.Ala18=) rs151027466 0.00009
NM_004064.5(CDKN1B):c.234G>A (p.Glu78=) rs751794433 0.00007
NM_004064.5(CDKN1B):c.225G>C (p.Glu75Asp) rs139727620 0.00006
NM_004064.5(CDKN1B):c.258G>A (p.Glu86=) rs142940486 0.00006
NM_004064.5(CDKN1B):c.530G>C (p.Gly177Ala) rs146167605 0.00006
NM_004064.5(CDKN1B):c.476-13C>T rs201069255 0.00005
NM_004064.5(CDKN1B):c.163G>A (p.Ala55Thr) rs759665516 0.00004
NM_004064.5(CDKN1B):c.*173T>C rs762188974 0.00003
NM_004064.5(CDKN1B):c.154A>C (p.Met52Leu) rs760647541 0.00003
NM_004064.5(CDKN1B):c.246C>T (p.Gly82=) rs376624980 0.00003
NM_004064.5(CDKN1B):c.-411T>C rs544835565 0.00001
NM_004064.5(CDKN1B):c.282C>T (p.Pro94=) rs751288223 0.00001
NM_004064.5(CDKN1B):c.308C>T (p.Ala103Val) rs773436050 0.00001
NM_004064.5(CDKN1B):c.365C>T (p.Pro122Leu) rs146973564 0.00001
NM_004064.5(CDKN1B):c.475+5T>C rs781394293 0.00001
NM_004064.5(CDKN1B):c.*610T>A rs4251698
NM_004064.5(CDKN1B):c.*96C>G rs556751200
NM_004064.5(CDKN1B):c.-254C>G rs561344485
NM_004064.5(CDKN1B):c.-7G>A rs751341214
NM_004064.5(CDKN1B):c.277C>T (p.Arg93Trp) rs140167393
NM_004064.5(CDKN1B):c.283C>G (p.Pro95Ala) rs188579132
NM_004064.5(CDKN1B):c.326T>A (p.Val109Asp) rs2066827
NM_004064.5(CDKN1B):c.367G>A (p.Ala123Thr) rs1946496773
NM_004064.5(CDKN1B):c.397C>A (p.Pro133Thr) rs137985549
NM_004064.5(CDKN1B):c.426G>C (p.Thr142=) rs149775942
NM_004064.5(CDKN1B):c.464C>A (p.Pro155His) rs143879243
NM_004064.5(CDKN1B):c.476-5C>G rs370509436
NM_004064.5(CDKN1B):c.476-6_476-5delinsAT rs1555085703

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