MSH6 c.2302C>G ;(p.P768A)

Variant ID: 2-48027424-C-G

NM_000179.2(MSH6):c.2302C>G;(p.P768A)

This variant was identified in 3 publications

View GRCh38 version.




Publications:


Germline mutations in penetrant cancer predisposition genes are rare in men with prostate cancer selecting active surveillance.

Cancer Medicine
Brady, Lauren L; Newcomb, Lisa F LF; Zhu, Kehao K; Zheng, Yingye Y; Boyer, Hilary H; Sarkar, Navonil De N; McKenney, Jesse K JK; Brooks, James D JD; Carroll, Peter R PR; Dash, Atreya A; Ellis, William J WJ; Filson, Christopher P CP; Gleave, Martin E ME; Liss, Michael A MA; Martin, Frances F; Morgan, Todd M TM; Thompson, Ian M IM; Wagner, Andrew A AA; Pritchard, Colin C CC; Lin, Daniel W DW; Nelson, Peter S PS
Publication Date: 2022-11

Variant appearance in text: MSH6: 2302C>G; Pro768Ala
PubMed Link: 35467778
Variant Present in the following documents:
  • CAM4-11-4332-s001.xls, sheet 1
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: 2302C>G; Pro768Ala; rs35946687
PubMed Link: 34253785
Variant Present in the following documents:
  • 41598_2021_93715_MOESM2_ESM.xlsx, sheet 8
View BVdb publication page



Investigation on the role of nsSNPs in HNPCC genes--a bioinformatics approach.

Journal Of Biomedical Science
Doss, C George Priya CG; Sethumadhavan, Rao R
Publication Date: 2009-04-24

Variant appearance in text: rs35946687
PubMed Link: 19389263
Variant Present in the following documents:
  • Main text
  • 1423-0127-16-42.pdf
View BVdb publication page