Varaico: Literature-Extracted Genetic Variants

Gene:CDKN1B
Variant:p.W60*
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CDKN1B

NM_004064.5:p.W60*

Associated Papers

The landscape of germline variants in breast and colorectal cancer susceptibility genes in patients with pituitary tumours.

Orsmond A et al.

Journal of Neuro-oncology, 2025

Beyond MEN1, When to Think About MEN4? Retrospective Study on 5600 Patients in the French Population and Literature Review.

Chevalier B et al.

The Journal of Clinical Endocrinology and Metabolism, 2024

Genomic landscape and tumor mutational features of resected preinvasive to invasive lung adenocarcinoma.

Lin Y et al.

Frontiers in Oncology, 2024

38803537 (PubMed )
Supplement: Table_1.xlsx › Table_S4

Novel germline variants of CDKN1B and CDKN2C identified during screening for familial primary hyperparathyroidism.

Mazarico-Altisent I et al.

Journal of Endocrinological Investigation, 2023

36334246 (PubMed )
Supplement: 40618_2022_1948_MOESM1_ESM.xlsx › Supplementary_material

MEN4, the MEN1 Mimicker: A Case Series of three Phenotypically Heterogenous Patients With Unique CDKN1B Mutations.

Seabrook A et al.

The Journal of Clinical Endocrinology and Metabolism, 2022

High prevalence of somatic PIK3CA and TP53 pathogenic variants in the normal mammary gland tissue of sporadic breast cancer patients revealed by duplex sequencing.

Kostecka A et al.

Npj Breast Cancer, 2022

35768433 (PubMed )
Supplement: 41523_2022_443_MOESM5_ESM.xlsx › Truncating_variants

Deciphering Genetic Alterations of Hairy Cell Leukemia and Hairy Cell Leukemia-like Disorders in 98 Patients.

Maitre E et al.

Cancers, 2022

35454811 (PubMed )
Supplement: cancers-14-01904-s001.zip › cancers-1638957-Supplementary › Supplementary_Table1.xlsx › mutations

Recurrent oligodendroglioma with changed 1p/19q status.

Barresi V et al.

Neuropathology : Official Journal of the Japanese Society of Neuropathology, 2022

35144313 (PubMed )
Supplement: NEUP-42-160-s001.xlsx › Foglio1

Landscape of CDKN1B Mutations in Luminal Breast Cancer and Other Hormone-Driven Human Tumors.

Cusan M et al.

Frontiers in Endocrinology, 2018

30065701 (PubMed )
Supplement: Table_1.XLSX › Foglio1

p27Kip1 and human cancers: A reappraisal of a still enigmatic protein.

Bencivenga D et al.

Cancer Letters, 2017

Recurrent CDKN1B (p27) mutations in hairy cell leukemia.

Dietrich S et al.

Blood, 2015

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Regarding the variants extracted from papers and shown text snippets from research papers, the following holds: "Some rights reserved. This work permits non-commercial use, distribution and reproduction in any medium, provided the original author and source are credited."