MSH6 c.1095G>A ;(p.W365*)

Variant ID: 2-48026217-G-A

NM_000179.2(MSH6):c.1095G>A;(p.W365*)

This variant was identified in 6 publications

View GRCh38 version.




Publications:


Novel preclinical gastroenteropancreatic neuroendocrine neoplasia models demonstrate the feasibility of mutation-based targeted therapy.

Cellular Oncology (Dordrecht)
Viol, Fabrice F; Sipos, Bence B; Fahl, Martina M; Clauditz, Till S TS; Amin, Tania T; Kriegs, Malte M; Nieser, Maike M; Izbicki, Jakob R JR; Huber, Samuel S; Lohse, Ansgar W AW; Schrader, Jörg J
Publication Date: 2022-10-21

Variant appearance in text: MSH6: 1095G>A
PubMed Link: 36269546
Variant Present in the following documents:
  • 13402_2022_Article_727.pdf
View BVdb publication page



Modeling biological and genetic diversity in upper tract urothelial carcinoma with patient derived xenografts.

Nature Communications
Kim, Kwanghee K; Hu, Wenhuo W; Audenet, François F; Almassi, Nima N; Hanrahan, Aphrothiti J AJ; Murray, Katie K; Bagrodia, Aditya A; Wong, Nathan N; Clinton, Timothy N TN; Dason, Shawn S; Mohan, Vishnu V; Jebiwott, Sylvia S; Nagar, Karan K; Gao, Jianjiong J; Penson, Alex A; Hughes, Chris C; Gordon, Benjamin B; Chen, Ziyu Z; Dong, Yiyu Y; Watson, Philip A PA; Alvim, Ricardo R; Elzein, Arijh A; Gao, Sizhi P SP; Cocco, Emiliano E; Santin, Alessandro D AD; Ostrovnaya, Irina I; Hsieh, James J JJ; Sagi, Irit I; Pietzak, Eugene J EJ; Hakimi, A Ari AA; Rosenberg, Jonathan E JE; Iyer, Gopa G; Vargas, Herbert A HA; Scaltriti, Maurizio M; Al-Ahmadie, Hikmat H; Solit, David B DB; Coleman, Jonathan A JA
Publication Date: 2020-04-24

Variant appearance in text: MSH6: 1095G>A; W365*
PubMed Link: 32332851
Variant Present in the following documents:
  • 41467_2020_15885_MOESM3_ESM.xlsx, sheet 3
  • 41467_2020_15885_MOESM3_ESM.xlsx, sheet 5
View BVdb publication page



Scarcity of Recurrent Regulatory Driver Mutations in Colorectal Cancer Revealed by Targeted Deep Sequencing.

Jnci Cancer Spectrum
Poulos, Rebecca C RC; Perera, Dilmi D; Packham, Deborah D; Shah, Anushi A; Janitz, Caroline C; Pimanda, John E JE; Hawkins, Nicholas N; Ward, Robyn L RL; Hesson, Luke B LB; Wong, Jason W H JWH
Publication Date: 2019-06

Variant appearance in text: MSH6: Trp365Ter
PubMed Link: 31360895
Variant Present in the following documents:
  • Main text
  • pkz012.pdf
View BVdb publication page



Distinctive DNA mismatch repair and APC rare variants in African Americans with colorectal neoplasia.

Oncotarget
Ashktorab, Hassan H; Azimi, Hamed H; Varma, Sudhir S; Tavakoli, Payaam P; Nickerson, Michael L ML; Brim, Hassan H
Publication Date: 2017-11-21

Variant appearance in text: MSH6: W365X
PubMed Link: 29245953
Variant Present in the following documents:
  • oncotarget-08-99966-s003.xlsx, sheet 2
View BVdb publication page



Reanalysis of BRCA1/2 negative high risk ovarian cancer patients reveals novel germline risk loci and insights into missing heritability.

Plos One
Stafford, Jaime L JL; Dyson, Gregory G; Levin, Nancy K NK; Chaudhry, Sophia S; Rosati, Rita R; Kalpage, Hasini H; Wernette, Courtney C; Petrucelli, Nancie N; Simon, Michael S MS; Tainsky, Michael A MA
Publication Date: 2017

Variant appearance in text: MSH6: W365*
PubMed Link: 28591191
Variant Present in the following documents:
  • pone.0178450.pdf
View BVdb publication page



Mismatch repair deficiency does not mediate clinical resistance to temozolomide in malignant glioma.

Clinical Cancer Research : An Official Journal Of The American Association For Cancer Research
Maxwell, Jill A JA; Johnson, Stewart P SP; McLendon, Roger E RE; Lister, David W DW; Horne, Krystle S KS; Rasheed, Ahmed A; Quinn, Jennifer A JA; Ali-Osman, Francis F; Friedman, Allan H AH; Modrich, Paul L PL; Bigner, Darell D DD; Friedman, Henry S HS
Publication Date: 2008-08-01

Variant appearance in text: MSH6: W365X
PubMed Link: 18676759
Variant Present in the following documents:
  • Main text
View BVdb publication page