Inferring Potential Cancer Driving Synonymous Variants

Synonymous single nucleotide variants (sSNVs) are often considered functionally silent, but a few cases of cancer-causing sSNVs have been reported. From available databases, we collected four categories of sSNVs: germline, somatic in normal tissues, somatic in cancerous tissues, and putative cancer...

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Detalles Bibliográficos
Autores principales: Zeng, Zishuo, Bromberg, Yana
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9140830/
https://www.ncbi.nlm.nih.gov/pubmed/35627162
http://dx.doi.org/10.3390/genes13050778

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9140830/
https://www.ncbi.nlm.nih.gov/pubmed/35627162
http://dx.doi.org/10.3390/genes13050778

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