CDH1 c.2400C>G ;(p.R800=)

Variant ID: 16-68863661-C-G

NM_004360.3(CDH1):c.2400C>G;(p.R800=)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Physician-directed genetic screening to evaluate personal risk for medically actionable disorders: a large multi-center cohort study.

Bmc Medicine
Haverfield, Eden V EV; Esplin, Edward D ED; Aguilar, Sienna J SJ; Hatchell, Kathryn E KE; Ormond, Kelly E KE; Hanson-Kahn, Andrea A; Atwal, Paldeep S PS; Macklin-Mantia, Sarah S; Hines, Stephanie S; Sak, Caron W-M CW; Tucker, Steven S; Bleyl, Steven B SB; Hulick, Peter J PJ; Gordon, Ora K OK; Velsher, Lea L; Gu, Jessica Y J JYJ; Weissman, Scott M SM; Kruisselbrink, Teresa T; Abel, Christopher C; Kettles, Michele M; Slavotinek, Anne A; Mendelsohn, Bryce A BA; Green, Robert C RC; Aradhya, Swaroop S; Nussbaum, Robert L RL
Publication Date: 2021-08-18

Variant appearance in text: CDH1: 2400C>G
PubMed Link: 34404389
Variant Present in the following documents:
  • 12916_2021_1999_MOESM2_ESM.pdf
View BVdb publication page



CDH1/E-cadherin germline mutations in early-onset gastric cancer.

Journal Of Medical Genetics
Bacani, J T JT; Soares, M M; Zwingerman, R R; di Nicola, N N; Senz, J J; Riddell, R R; Huntsman, D G DG; Gallinger, S S
Publication Date: 2006-11

Variant appearance in text: CDH1: R800R
PubMed Link: 16801346
Variant Present in the following documents:
  • Main text
View BVdb publication page