CDH1 c.2295+488T>A

Variant ID: 16-68862695-T-A

NM_004360.3(CDH1):c.2295+488T>A

This variant was identified in 1 publication

View GRCh38 version.



Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP

Publications:

A unified analytic framework for prioritization of non-coding variants of uncertain significance in heritable breast and ovarian cancer.

Bmc Medical Genomics
Mucaki, Eliseos J EJ; Caminsky, Natasha G NG; Perri, Ami M AM; Lu, Ruipeng R; Laederach, Alain A; Halvorsen, Matthew M; Knoll, Joan H M JH; Rogan, Peter K PK
Publication Date: 2016-04-11

Variant appearance in text: rs34927405
PubMed Link: 27067391
Variant Present in the following documents:
  • 12920_2016_178_MOESM14_ESM.xlsx, sheet 1
  • 12920_2016_178_MOESM13_ESM.xlsx, sheet 1
  • 12920_2016_178_MOESM8_ESM.xlsx, sheet 1
View BVdb publication page