Varaico: Literature-Extracted Genetic Variants

Gene:MSH2
Variant:p.A689D
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MSH2

NM_000251.3:p.A689D

Associated Papers

Detection of germline variants with pathogenic potential in 48 patients with familial colorectal cancer by using whole exome sequencing.

Singh AK et al.

Bmc Medical Genomics, 2023

The association of blood ctDNA levels to mutations of marker genes in colorectal cancer.

Bai F et al.

Cancer Reports (hoboken, N.j.), 2023

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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."