MLH1 c.588+3_588+6del

Variant ID: 3-37053351-AAAGT-A

NM_000249.3(MLH1):c.588+3_588+6del

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Multigene Panel Testing in Turkish Hereditary Cancer Syndrome Patients.

Medeniyet Medical Journal
Arslan Ates, Esra E; Turkyilmaz, Ayberk A; Alavanda, Ceren C; Yildirim, Ozlem O; Guney, Ahmet Ilter AI
Publication Date: 2022-06-23

Variant appearance in text: MLH1: 588+3_588+6del
PubMed Link: 35734982
Variant Present in the following documents:
  • medj-37-150.pdf
View BVdb publication page



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: MLH1: 588+3_588+6del
PubMed Link: 17453009
Variant Present in the following documents:
  • Main text
  • 6603754a.pdf
View BVdb publication page