ClinVar Miner

List of variants reported as benign for Multiple endocrine neoplasia type 4 by Illumina Laboratory Services, Illumina

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Total variants: 27
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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.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.*833T>A rs141549130 0.00298
NM_004064.5(CDKN1B):c.-126C>T rs549943001 0.00118
NM_004064.5(CDKN1B):c.165G>A (p.Ala55=) rs16908375 0.00068
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.-10C>T rs374913823 0.00009
NM_004064.5(CDKN1B):c.234G>A (p.Glu78=) rs751794433 0.00007
NM_004064.5(CDKN1B):c.258G>A (p.Glu86=) rs142940486 0.00006
NM_004064.5(CDKN1B):c.476-13C>T rs201069255 0.00005
NM_004064.5(CDKN1B):c.*173T>C rs762188974 0.00003
NM_004064.5(CDKN1B):c.-411T>C rs544835565 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.277C>T (p.Arg93Trp) rs140167393

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