ClinVar Miner

List of variants in gene CDKN1B reported as uncertain significance by GeneDx

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Total variants: 36
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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.407A>G (p.Asp136Gly) rs546234840 0.00020
NM_004064.5(CDKN1B):c.362C>T (p.Ala121Val) rs201685429 0.00016
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.530G>C (p.Gly177Ala) rs146167605 0.00006
NM_004064.5(CDKN1B):c.476A>G (p.Asp159Gly) rs893650334 0.00005
NM_004064.5(CDKN1B):c.25G>A (p.Gly9Arg) rs755225286 0.00004
NM_004064.5(CDKN1B):c.31C>T (p.Pro11Ser) rs779193240 0.00004
NM_004064.5(CDKN1B):c.35G>T (p.Ser12Ile) rs775772074 0.00003
NM_004064.5(CDKN1B):c.464C>G (p.Pro155Arg) rs143879243 0.00003
NM_004064.5(CDKN1B):c.349C>T (p.Pro117Ser) rs754936421 0.00002
NM_004064.5(CDKN1B):c.167G>C (p.Ser56Thr) rs758686055 0.00001
NM_004064.5(CDKN1B):c.267C>T (p.Tyr89=) rs532903617 0.00001
NM_004064.5(CDKN1B):c.271C>A (p.Pro91Thr) rs769828807 0.00001
NM_004064.5(CDKN1B):c.285C>A (p.Pro95=) rs780148172 0.00001
NM_004064.5(CDKN1B):c.386A>G (p.His129Arg) rs766996989 0.00001
NM_004064.5(CDKN1B):c.410C>T (p.Pro137Leu) rs369871673 0.00001
NM_004064.5(CDKN1B):c.-17G>A
NM_004064.5(CDKN1B):c.-31AG[1] rs774454456
NM_004064.5(CDKN1B):c.-36G>C
NM_004064.5(CDKN1B):c.-7G>A rs751341214
NM_004064.5(CDKN1B):c.-9G>A
NM_004064.5(CDKN1B):c.199C>G (p.His67Asp) rs867208075
NM_004064.5(CDKN1B):c.205C>G (p.Pro69Ala) rs1388968180
NM_004064.5(CDKN1B):c.272C>G (p.Pro91Arg) rs768793049
NM_004064.5(CDKN1B):c.283C>T (p.Pro95Ser) rs188579132
NM_004064.5(CDKN1B):c.29G>C (p.Ser10Thr) rs1555085482
NM_004064.5(CDKN1B):c.394G>C (p.Asp132His) rs760403492
NM_004064.5(CDKN1B):c.416A>T (p.Asp139Val)
NM_004064.5(CDKN1B):c.485C>T (p.Thr162Ile) rs774965131
NM_004064.5(CDKN1B):c.83C>T (p.Ala28Val) rs1592280774

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