Varaico: Literature-Extracted Genetic Variants

Gene:MSH2
Variant:p.S323F
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MSH2

NM_000251.3:p.S323F

Associated Papers

Whole-exome Sequencing of Nigerian Prostate Tumors from the Prostate Cancer Transatlantic Consortium (CaPTC) Reveals DNA Repair Genes Associated with African Ancestry.

White JA et al.

Cancer Research Communications, 2022

36922933 (PubMed )
Supplement: crc-22-0136-s01.xlsx › ST1_Known_Germline_Variants

Prevalence and spectrum of DNA mismatch repair gene variation in the general Chinese population.

Zhang L et al.

Journal of Medical Genetics, 2022

34172528 (PubMed )
Supplement: jmedgenet-2021-107886supp003.xlsx › MSH2

Genomic deletions in MSH2 or MLH1 are a frequent cause of hereditary non-polyposis colorectal cancer: identification of novel and recurrent deletions by MLPA.

Taylor CF et al.

Human Mutation, 2003

Novel genomic prognostic biomarkers for dogs with cancer.

Chon E et al.

Journal of Veterinary Internal Medicine, 0

37801037 (PubMed )
Supplement: JVIM-37-2410-s001.xlsx › Supp._Table_1
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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."