MSH2 c.2665_2666delinsGG ;(p.S889G)

Variant ID: 2-47709948-TC-GG

NM_000251.2(MSH2):c.2665_2666delinsGG;(p.S889G)

This variant was identified in 3 publications

View GRCh38 version.




Publications:


Assessment of Clinical Benefit of Integrative Genomic Profiling in Advanced Solid Tumors.

Jama Oncology
Cobain, Erin F EF; Wu, Yi-Mi YM; Vats, Pankaj P; Chugh, Rashmi R; Worden, Francis F; Smith, David C DC; Schuetze, Scott M SM; Zalupski, Mark M MM; Sahai, Vaibhav V; Alva, Ajjai A; Schott, Anne F AF; Caram, Megan E V MEV; Hayes, Daniel F DF; Stoffel, Elena M EM; Jacobs, Michelle F MF; Kumar-Sinha, Chandan C; Cao, Xuhong X; Wang, Rui R; Lucas, David D; Ning, Yu Y; Rabban, Erica E; Bell, Janice J; Camelo-Piragua, Sandra S; Udager, Aaron M AM; Cieslik, Marcin M; Lonigro, Robert J RJ; Kunju, Lakshmi P LP; Robinson, Dan R DR; Talpaz, Moshe M; Chinnaiyan, Arul M AM
Publication Date: 2021-04-01

Variant appearance in text: MSH2: S889G
PubMed Link: 33630025
Variant Present in the following documents:
  • jamaoncol-e207987-s004.xlsx, sheet 2
View BVdb publication page



Characterization of Clonal Evolution in Microsatellite Unstable Metastatic Cancers through Multiregional Tumor Sequencing.

Molecular Cancer Research : Mcr
Bonneville, Russell R; Paruchuri, Anoosha A; Wing, Michele R MR; Krook, Melanie A MA; Reeser, Julie W JW; Chen, Hui-Zi HZ; Dao, Thuy T; Samorodnitsky, Eric E; Smith, Amy M AM; Yu, Lianbo L; Nowacki, Nicholas N; Chen, Wei W; Roychowdhury, Sameek S
Publication Date: 2021-03

Variant appearance in text: MSH2: S889G
PubMed Link: 33229401
Variant Present in the following documents:
  • Main text
View BVdb publication page



Clinical application of a cancer genomic profiling assay to guide precision medicine decisions.

Personalized Medicine
Eifert, Cheryl C; Pantazi, Angeliki A; Sun, Ruobai R; Xu, Jia J; Cingolani, Pablo P; Heyer, Joerg J; Russell, Meaghan M; Lvova, Maria M; Ring, Jennifer J; Tse, Julie Y JY; Lyle, Stephen S; Protopopov, Alexei A
Publication Date: 2017-07

Variant appearance in text: MSH2: S889G
PubMed Link: 28890729
Variant Present in the following documents:
  • Main text
View BVdb publication page