MSH2 c.667_668delinsGC ;(p.L223A)

Variant ID: 2-47639574-CT-GC

NM_000251.2(MSH2):c.667_668delinsGC;(p.L223A)

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: L223A
PubMed Link: 31819097
Variant Present in the following documents:
  • 41598_2019_54976_MOESM2_ESM.xlsx, sheet 8
View BVdb publication page



Colorectal polyposis and inherited colorectal cancer syndromes.

Annals Of Gastroenterology
Byrne, Raphael M RM; Tsikitis, Vassiliki Liana VL
Publication Date: 2018

Variant appearance in text: MSH2: L223A
PubMed Link: 29333064
Variant Present in the following documents:
  • Main text
  • AnnGastroenterol-31-24.pdf
View BVdb publication page