MSH6 c.597del ;(p.S200Qfs*11)

Variant ID: 2-48023169-GC-G

NM_000179.2(MSH6):c.597del;(p.S200Qfs*11)

This variant was identified in 3 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: 597del; Ser200fs
PubMed Link: 36823319
Variant Present in the following documents:
  • 41588_2023_1327_MOESM4_ESM.xlsx, sheet 6
View BVdb publication page



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: MSH6: 597del; Ser200Glnfs
PubMed Link: 34253785
Variant Present in the following documents:
  • 41598_2021_93715_MOESM2_ESM.xlsx, sheet 7
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: MSH6: 595_595delC; Ser200fs
PubMed Link: 32587781
Variant Present in the following documents:
  • Main text
  • cbm-17-458.pdf
View BVdb publication page