CDH1 c.35T>C ;(p.L12P)

Variant ID: 16-68771353-T-C

NM_004360.3(CDH1):c.35T>C;(p.L12P)

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:

Interference with Sin3 function induces epigenetic reprogramming and differentiation in breast cancer cells.

Proceedings Of The National Academy Of Sciences Of The United States Of America
Farias, Eduardo F EF; Petrie, Kevin K; Leibovitch, Boris B; Murtagh, Janice J; Chornet, Manuel Boix MB; Schenk, Tino T; Zelent, Arthur A; Waxman, Samuel S
Publication Date: 2010-06-29

Variant appearance in text: CDH1: L12P
PubMed Link: 20547842
Variant Present in the following documents:
  • Main text
View BVdb publication page