ClinVar Miner

List of variants in gene CDKN1B reported as benign by Ambry Genetics

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Total variants: 23
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HGVS dbSNP gnomAD frequency
NM_004064.5(CDKN1B):c.326T>G (p.Val109Gly) rs2066827 0.36014
NM_004064.5(CDKN1B):c.577C>T (p.Leu193Phe) rs73281150 0.00338
NM_004064.5(CDKN1B):c.165G>A (p.Ala55=) rs16908375 0.00068
NM_004064.5(CDKN1B):c.356T>C (p.Ile119Thr) rs142833529 0.00057
NM_004064.5(CDKN1B):c.155T>G (p.Met52Arg) rs543122580 0.00037
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.281C>T (p.Pro94Leu) rs757917082 0.00011
NM_004064.5(CDKN1B):c.125C>T (p.Thr42Ile) rs200422211 0.00009
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.163G>A (p.Ala55Thr) rs759665516 0.00004
NM_004064.5(CDKN1B):c.154A>C (p.Met52Leu) rs760647541 0.00003
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.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.397C>A (p.Pro133Thr) rs137985549
NM_004064.5(CDKN1B):c.464C>A (p.Pro155His) rs143879243
NM_004064.5(CDKN1B):c.476-6_476-5delinsAT rs1555085703

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