MSH6 c.628-7C>A

Variant ID: 2-48025743-C-A

NM_000179.2(MSH6):c.628-7C>A

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Prevalence of germline pathogenic variants in 22 cancer susceptibility genes in Swedish pediatric cancer patients.

Scientific Reports
von Stedingk, Kristoffer K; Stjernfelt, Karl-Johan KJ; Kvist, Anders A; Wahlström, Cecilia C; Kristoffersson, Ulf U; Stenmark-Askmalm, Marie M; Wiebe, Thomas T; Hjorth, Lars L; Koster, Jan J; Olsson, Håkan H; Øra, Ingrid I
Publication Date: 2021-03-05

Variant appearance in text: MSH6: 628-7C>A; rs373129248
PubMed Link: 33674644
Variant Present in the following documents:
  • 41598_2021_84502_MOESM2_ESM.xlsx, sheet 10
View BVdb publication page



Targeted sequencing of genes associated with the mismatch repair pathway in patients with endometrial cancer.

Plos One
Singh, Ashish Kumar AK; Talseth-Palmer, Bente B; McPhillips, Mary M; Lavik, Liss Anne Solberg LAS; Xavier, Alexandre A; Drabløs, Finn F; Sjursen, Wenche W
Publication Date: 2020

Variant appearance in text: MSH6: 628-7C>A; rs373129248
PubMed Link: 32634176
Variant Present in the following documents:
  • Main text
  • pone.0235613.s008.xlsx, sheet 1
  • pone.0235613.pdf
View BVdb publication page