MSH6 c.648A>C ;(p.T216=)

Variant ID: 2-48025770-A-C

NM_000179.2(MSH6):c.648A>C;(p.T216=)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Targeted exome sequencing reveals distinct pathogenic variants in Iranians with colorectal cancer.

Oncotarget
Ashktorab, Hassan H; Mokarram, Pooneh P; Azimi, Hamed H; Olumi, Hasti H; Varma, Sudhir S; Nickerson, Michael L ML; Brim, Hassan H
Publication Date: 2017-01-31

Variant appearance in text: MSH6: T216T
PubMed Link: 28002797
Variant Present in the following documents:
  • oncotarget-08-7852-s002.xlsx, sheet 13
View BVdb publication page



MSH6 germline mutations in early-onset colorectal cancer patients without family history of the disease.

British Journal Of Cancer
Pinto, C C; Veiga, I I; Pinheiro, M M; Mesquita, B B; Jeronimo, C C; Sousa, O O; Fragoso, M M; Santos, L L; Moreira-Dias, L L; Baptista, M M; Lopes, C C; Castedo, S S; Teixeira, M R MR
Publication Date: 2006-09-18

Variant appearance in text: MSH6: T216T
PubMed Link: 16940983
Variant Present in the following documents:
  • Main text
  • 95-6603318a.pdf
View BVdb publication page