ClinVar Miner

Variants in gene CDKN1B with conflicting interpretations "likely benign" and "uncertain significance"

Submission 1 (likely benign) minimum review status: Submission 1 (likely benign) method:
Submission 2 (uncertain significance) minimum review status: Submission 2 (uncertain significance) method:
Gene type:
ClinVar version:
Total variants with conflicting interpretations: 18
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HGVS dbSNP gnomAD frequency
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.-80C>T rs551236750 0.00021
NM_004064.5(CDKN1B):c.407A>G (p.Asp136Gly) rs546234840 0.00020
NM_004064.5(CDKN1B):c.482C>G (p.Ser161Cys) rs373917399 0.00014
NM_004064.5(CDKN1B):c.54C>T (p.Ala18=) rs151027466 0.00009
NM_004064.5(CDKN1B):c.225G>C (p.Glu75Asp) rs139727620 0.00006
NM_004064.5(CDKN1B):c.216C>T (p.Gly72=) rs776643344 0.00004
NM_004064.5(CDKN1B):c.279G>A (p.Arg93=) rs766901538 0.00001
NM_004064.5(CDKN1B):c.-31AG[1] rs774454456
NM_004064.5(CDKN1B):c.271C>T (p.Pro91Ser) rs769828807
NM_004064.5(CDKN1B):c.27G>A (p.Gly9=) rs1060503869
NM_004064.5(CDKN1B):c.326T>A (p.Val109Asp) rs2066827
NM_004064.5(CDKN1B):c.372C>T (p.Asn124=) rs760081465
NM_004064.5(CDKN1B):c.397C>A (p.Pro133Thr) rs137985549
NM_004064.5(CDKN1B):c.449G>C (p.Gly150Ala) rs772818396
NM_004064.5(CDKN1B):c.485C>T (p.Thr162Ile) rs774965131

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