MLH1 c.110A>G ;(p.E37G)

Variant ID: 3-37035148-A-G

NM_000249.3(MLH1):c.110A>G;(p.E37G)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


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: HNPCC2: E37G
PubMed Link: 34253785
Variant Present in the following documents:
  • 41598_2021_93715_MOESM3_ESM.xlsx, sheet 4
  • 41598_2021_93715_MOESM2_ESM.xlsx, sheet 8
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DNA Mismatch Repair Deficiency in Rectal Cancer: Benchmarking Its Impact on Prognosis, Neoadjuvant Response Prediction, and Clinical Cancer Genetics.

Journal Of Clinical Oncology : Official Journal Of The American Society Of Clinical Oncology
de Rosa, Nicole N; Rodriguez-Bigas, Miguel A MA; Chang, George J GJ; Veerapong, Jula J; Borras, Ester E; Krishnan, Sunil S; Bednarski, Brian B; Messick, Craig A CA; Skibber, John M JM; Feig, Barry W BW; Lynch, Patrick M PM; Vilar, Eduardo E; You, Y Nancy YN
Publication Date: 2016-09-01

Variant appearance in text: MLH1: 110A>G; E37G
PubMed Link: 27432916
Variant Present in the following documents:
  • Main text
View BVdb publication page