MSH2 c.2092G>T ;(p.E698*)

Variant ID: 2-47703592-G-T

NM_000251.2(MSH2):c.2092G>T;(p.E698*)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Low neoantigen expression and poor T-cell priming underlie early immune escape in colorectal cancer.

Nature Cancer
Westcott, Peter M K PMK; Sacks, Nathan J NJ; Schenkel, Jason M JM; Ely, Zackery A ZA; Smith, Olivia O; Hauck, Haley H; Jaeger, Alex M AM; Zhang, Daniel D; Backlund, Coralie M CM; Beytagh, Mary C MC; Patten, J J JJ; Elbashir, Ryan R; Eng, George G; Irvine, Darrell J DJ; Yilmaz, Omer H OH; Jacks, Tyler T
Publication Date: 2021-10

Variant appearance in text: MSH2: 2092G>T
PubMed Link: 34738089
Variant Present in the following documents:
  • NIHMS1725490-supplement-Source_Data_Figure_1.xlsx, sheet 1
View BVdb publication page



Identification of novel Lynch syndrome mutations in Chinese patients with endometriod endometrial cancer.

Cancer Biology & Medicine
Ren, Caixia C; Liu, Yan Y; Wang, Yuxiang Y; Tang, Yan Y; Wei, Yawei Y; Liu, Congrong C; Zhang, Hongquan H
Publication Date: 2020-05-15

Variant appearance in text: MSH2: 2092G>T; Glu698Ter
PubMed Link: 32587781
Variant Present in the following documents:
  • Main text
  • cbm-17-458.pdf
View BVdb publication page