CDH1 c.2295+2T>G

Variant ID: 16-68862209-T-G

NM_004360.3(CDH1):c.2295+2T>G

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Associations of CDH1 germline variant location and cancer phenotype in families with hereditary diffuse gastric cancer (HDGC).

Journal Of Medical Genetics
Lo, Winifred W; Zhu, Bin B; Sabesan, Arvind A; Wu, Ho-Hsiang HH; Powers, Astin A; Sorber, Rebecca A RA; Ravichandran, Sarangan S; Chen, Ina I; McDuffie, Lucas A LA; Quadri, Humair S HS; Beane, Joal D JD; Calzone, Kathleen K; Miettinen, Markku M MM; Hewitt, Stephen M SM; Koh, Christopher C; Heller, Theo T; Wacholder, Sholom S; Rudloff, Udo U
Publication Date: 2019-06

Variant appearance in text: CDH1: 2295+2T>G
PubMed Link: 30745422
Variant Present in the following documents:
  • Main text
View BVdb publication page