CDH1 c.1689C>A ;(p.A563=)

Variant ID: 16-68853306-C-A

NM_004360.3(CDH1):c.1689C>A;(p.A563=)

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: CDH1: Ala563=; rs587780786
PubMed Link: 33674644
Variant Present in the following documents:
  • 41598_2021_84502_MOESM2_ESM.xlsx, sheet 10
View BVdb publication page



Somatic sequence alterations in twenty-one genes selected by expression profile analysis of breast carcinomas.

Breast Cancer Research : Bcr
Chanock, Stephen J SJ; Burdett, Laurie L; Yeager, Meredith M; Llaca, Victor V; Langerød, Anita A; Presswalla, Shafaq S; Kaaresen, Rolf R; Strausberg, Robert L RL; Gerhard, Daniela S DS; Kristensen, Vessela V; Perou, Charles M CM; Børresen-Dale, Anne-Lise AL
Publication Date: 2007

Variant appearance in text: CDH1: A563A
PubMed Link: 17224074
Variant Present in the following documents:
  • Main text
  • bcr1637.pdf
View BVdb publication page