MSH6 c.866G>C ;(p.G289A)

Variant ID: 2-48025988-G-C

NM_000179.2(MSH6):c.866G>C;(p.G289A)

This variant was identified in 3 publications

View GRCh38 version.




Publications:


OncoPanĀ®: An NGS-Based Screening Methodology to Identify Molecular Markers for Therapy and Risk Assessment in Pancreatic Ductal Adenocarcinoma.

Biomedicines
Tibiletti, Maria Grazia MG; Carnevali, Ileana I; Pensotti, Valeria V; Chiaravalli, Anna Maria AM; Facchi, Sofia S; Volorio, Sara S; Mariette, Frederique F; Mariani, Paolo P; Fortuzzi, Stefano S; Pierotti, Marco Alessandro MA; Sessa, Fausto F
Publication Date: 2022-05-23

Variant appearance in text: MSH6: 866G>C; Gly289Ala
PubMed Link: 35625944
Variant Present in the following documents:
  • biomedicines-10-01208.pdf
View BVdb publication page



A computational and structural analysis of germline and somatic variants affecting the DDR mechanism, and their impact on human diseases.

Scientific Reports
Magraner-Pardo, Lorena L; Laskowski, Roman A RA; Pons, Tirso T; Thornton, Janet M JM
Publication Date: 2021-07-12

Variant appearance in text: MSH6: 866G>C; Gly289Ala; rs368318845
PubMed Link: 34253785
Variant Present in the following documents:
  • 41598_2021_93715_MOESM2_ESM.xlsx, sheet 8
View BVdb publication page



MutS Homologues hMSH4 and hMSH5: Genetic Variations, Functions, and Implications in Human Diseases.

Current Genomics
Clark, Nicole N; Wu, Xiling X; Her, Chengtao C
Publication Date: 2013-04

Variant appearance in text: MSH6: G289A
PubMed Link: 24082819
Variant Present in the following documents:
  • Main text
View BVdb publication page