Varaico: Literature-Extracted Genetic Variants

Gene:FANCD2
Variant:p.K871N
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FANCD2

NM_001018115.3:p.K871N

Associated Papers

Human papillomavirus integration perspective in small cell cervical carcinoma.

Wang X et al.

Nature Communications, 2022

36216793 (PubMed )
Supplement: 41467_2022_33359_MOESM21_ESM.xlsx › Supplementary_Data18

PRMT1-dependent regulation of RNA metabolism and DNA damage response sustains pancreatic ductal adenocarcinoma.

Giuliani V et al.

Nature Communications, 2021

34330913 (PubMed )
Supplement: 41467_2021_24798_MOESM3_ESM.xlsx › exome_data

Epithelial Cells of Deep Infiltrating Endometriosis Harbor Mutations in Cancer Driver Genes.

Koppolu A et al.

Cells, 2021

Mutational landscape and genetic signatures of cell-free DNA in tumour-induced osteomalacia.

Wu N et al.

Journal of Cellular and Molecular Medicine, 2020

32277576 (PubMed )
Supplement: JCMM-24-4931-s011.xlsx › Sheet1

PTEN deletion drives acute myeloid leukemia resistance to MEK inhibitors.

Smith AM et al.

Oncotarget, 2019

31645898 (PubMed )
Supplement: oncotarget-10-5755-s003.xlsx › Sheet1

Mutational landscape of radiation-associated angiosarcoma of the breast.

Thibodeau BJ et al.

Oncotarget, 2018

Comprehensive whole genome sequence analyses yields novel genetic and structural insights for Intellectual Disability.

Zahir FR et al.

Bmc Genomics, 2017

28539120 (PubMed )
Supplement: 12864_2017_3671_MOESM8_ESM.xlsx › Patient_59

SeqHBase: a big data toolset for family based sequencing data analysis.

He M et al.

Journal of Medical Genetics, 2015

25587064 (PubMed )
Supplement: jmedgenet-2014-102907-s1.pdf
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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."