MSH6 c.3029C>G ;(p.T1010S)

Variant ID: 2-48028151-C-G

NM_000179.2(MSH6):c.3029C>G;(p.T1010S)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Rates of Variants of Uncertain Significance Among Patients With Breast Cancer Undergoing Genetic Testing: Regional Perspectives.

Frontiers In Oncology
Abdel-Razeq, Hikmat H; Tamimi, Faris F; Abujamous, Lama L; Abdel-Razeq, Rashid R; Abunasser, Mahmoud M; Edaily, Sara S; Abdulelah, Hazem H; Khashabeh, Razan Abu RA; Bater, Rayan R
Publication Date: 2022

Variant appearance in text: MSH6: 3029C>G; Thr1010Ser
PubMed Link: 35402282
Variant Present in the following documents:
  • Main text
  • fonc-12-673094.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: 3029C>G; Thr1010Ser
PubMed Link: 34253785
Variant Present in the following documents:
  • 41598_2021_93715_MOESM2_ESM.xlsx, sheet 8
View BVdb publication page