MSH2 c.115_117delinsAGC ;(p.R39S)

Variant ID: 2-47630445-CGG-AGC

NM_000251.2(MSH2):c.115_117delinsAGC;(p.R39S)

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: R39S
PubMed Link: 31819097
Variant Present in the following documents:
  • 41598_2019_54976_MOESM2_ESM.xlsx, sheet 8
View BVdb publication page



Molecular epidemiology of DNA repair gene polymorphisms and head and neck cancer.

Journal Of Biomedical Research
Wang, Meilin M; Chu, Haiyan H; Zhang, Zhengdong Z; Wei, Qingyi Q
Publication Date: 2013-05

Variant appearance in text: MSH2: Arg39Ser
PubMed Link: 23720673
Variant Present in the following documents:
  • Main text
View BVdb publication page