MSH6 c.425G>A ;(p.W142*)

Variant ID: 2-48018230-G-A

NM_000179.2(MSH6):c.425G>A;(p.W142*)

This variant was identified in 5 publications

View GRCh38 version.




Publications:


Network expansion of genetic associations defines a pleiotropy map of human cell biology.

Nature Genetics
Barrio-Hernandez, Inigo I; Schwartzentruber, Jeremy J; Shrivastava, Anjali A; Del-Toro, Noemi N; Gonzalez, Asier A; Zhang, Qian Q; Mountjoy, Edward E; Suveges, Daniel D; Ochoa, David D; Ghoussaini, Maya M; Bradley, Glyn G; Hermjakob, Henning H; Orchard, Sandra S; Dunham, Ian I; Anderson, Carl A CA; Porras, Pablo P; Beltrao, Pedro P
Publication Date: 2023-02-23

Variant appearance in text: MSH6: 425G>A; Trp142Ter
PubMed Link: 36823319
Variant Present in the following documents:
  • 41588_2023_1327_MOESM4_ESM.xlsx, sheet 6
View BVdb publication page



Temozolomide Treatment Alters Mismatch Repair and Boosts Mutational Burden in Tumor and Blood of Colorectal Cancer Patients.

Cancer Discovery
Crisafulli, Giovanni G; Sartore-Bianchi, Andrea A; Lazzari, Luca L; Pietrantonio, Filippo F; Amatu, Alessio A; Macagno, Marco M; Barault, Ludovic L; Cassingena, Andrea A; Bartolini, Alice A; Luraghi, Paolo P; Mauri, Gianluca G; Battuello, Paolo P; Personeni, Nicola N; Zampino, Maria Giulia MG; Pessei, Valeria V; Vitiello, Pietro Paolo PP; Tosi, Federica F; Idotta, Laura L; Morano, Federica F; Valtorta, Emanuele E; Bonoldi, Emanuela E; Germano, Giovanni G; Di Nicolantonio, Federica F; Marsoni, Silvia S; Siena, Salvatore S; Bardelli, Alberto A
Publication Date: 2022-07-06

Variant appearance in text: MSH6: W142*
PubMed Link: 35522273
Variant Present in the following documents:
  • cd-21-1434_supplementary_figures_and_tables_suppsf1-sf7st1-st3.pdf
  • 1656.pdf
View BVdb publication page



Pathogenic Variant Profile of Hereditary Cancer Syndromes in a Vietnamese Cohort.

Frontiers In Oncology
Tran, Van Thuan VT; Nguyen, Sao Trung ST; Pham, Xuan Dung XD; Phan, Thanh Hai TH; Nguyen, Van Chu VC; Nguyen, Huu Thinh HT; Nguyen, Huu Phuc HP; Doan, Phuong Thao Thi PTT; Le, Tuan Anh TA; Nguyen, Bao Toan BT; Jasmine, Thanh Xuan TX; Nguyen, Duy Sinh DS; Nguyen, Hong-Dang Luu HL; Nguyen, Ngoc Mai NM; Do, Duy Xuan DX; Tran, Vu Uyen VU; Nguyen, Hue Hanh Thi HHT; Le, Minh Phong MP; Nguyen, Yen Nhi YN; Do, Thanh Thuy Thi TTT; Truong, Dinh Kiet DK; Tang, Hung Sang HS; Phan, Minh-Duy MD; Nguyen, Hoai-Nghia HN; Giang, Hoa H; Tu, Lan N LN
Publication Date: 2021

Variant appearance in text: MSH6: 425G>A; Trp142Ter
PubMed Link: 35070997
Variant Present in the following documents:
  • Main text
  • fonc-11-789659.pdf
View BVdb publication page



Prevalence and spectrum of germline cancer susceptibility gene variants and somatic second hits in colorectal cancer.

American Journal Of Cancer Research
Liao, Haiyan H; Cai, Songhua S; Bai, Yuezong Y; Zhang, Bei B; Sheng, Yuling Y; Tong, Shuang S; Cai, Jinping J; Zhao, Feilong F; Zhao, Xiaochen X; Chen, Shiqing S; Zhang, Cheng C; Gao, Jing J
Publication Date: 2021

Variant appearance in text: MSH6: 425G>A
PubMed Link: 34873480
Variant Present in the following documents:
  • Main text
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: W142X
PubMed Link: 29245953
Variant Present in the following documents:
  • oncotarget-08-99966-s003.xlsx, sheet 2
View BVdb publication page