MSH6 c.836del ;(p.S279Tfs*12)

Variant ID: 2-48025958-AG-A

NM_000179.2(MSH6):c.836del;(p.S279Tfs*12)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Patients with an unexplained microsatellite instable tumour have a low risk of familial cancer.

British Journal Of Cancer
Overbeek, L I H LI; Kets, C M CM; Hebeda, K M KM; Bodmer, D D; van der Looij, E E; Willems, R R; Goossens, M M; Arts, N N; Brunner, H G HG; van Krieken, J H J M JH; Hoogerbrugge, N N; Ligtenberg, M J L MJ
Publication Date: 2007-05-21

Variant appearance in text: MSH6: 836del
PubMed Link: 17453009
Variant Present in the following documents:
  • Main text
View BVdb publication page