MSH2 c.1021_1022delinsGC ;(p.L341A)

Variant ID: 2-47643513-CT-GC

NM_000251.2(MSH2):c.1021_1022delinsGC;(p.L341A)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Refinement of evolutionary medicine predictions based on clinical evidence for the manifestations of Mendelian diseases.

Scientific Reports
Šimčíková, Daniela D; Heneberg, Petr P
Publication Date: 2019-12-09

Variant appearance in text: MSH2: L341A
PubMed Link: 31819097
Variant Present in the following documents:
  • 41598_2019_54976_MOESM2_ESM.xlsx, sheet 8
View BVdb publication page



Evolutionary Covariance Combined with Molecular Dynamics Predicts a Framework for Allostery in the MutS DNA Mismatch Repair Protein.

The Journal Of Physical Chemistry. B
Lakhani, Bharat B; Thayer, Kelly M KM; Hingorani, Manju M MM; Beveridge, David L DL
Publication Date: 2017-03-09

Variant appearance in text: MSH2: L341A
PubMed Link: 28135092
Variant Present in the following documents:
  • Main text
  • jp6b11976_si_001.pdf
View BVdb publication page