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CDH1 c.1460T>C ;(p.V487A)
Variant ID: 16-68849557-T-C
NM_004360.3(
CDH1
):c.1460T>C;(p.V487A)
This variant was identified in 3 publications
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
Publications:
Roles for E-cadherin cell surface regulation in cancer.
Molecular Biology Of The Cell
Petrova, Yuliya I YI; Schecterson, Leslayann L; Gumbiner, Barry M BM
Publication Date: 2016-11-01
Variant appearance in text: CDH1: V487A
PubMed Link:
27582386
Variant Present in the following documents:
Main text
3233.pdf
View BVdb publication page
GESPA: classifying nsSNPs to predict disease association.
Bmc Bioinformatics
Khurana, Jay K JK; Reeder, Jay E JE; Shrimpton, Antony E AE; Thakar, Juilee J
Publication Date: 2015-07-25
Variant appearance in text: CDH1: V487A
PubMed Link:
26206375
Variant Present in the following documents:
12859_2015_673_MOESM1_ESM.xls, sheet 4
View BVdb publication page
E-cadherin destabilization accounts for the pathogenicity of missense mutations in hereditary diffuse gastric cancer.
Plos One
Simões-Correia, Joana J; Figueiredo, Joana J; Lopes, Rui R; Stricher, François F; Oliveira, Carla C; Serrano, Luis L; Seruca, Raquel R
Publication Date: 2012
Variant appearance in text: CDH1: V487A
PubMed Link:
22470475
Variant Present in the following documents:
Main text
pone.0033783.pdf
View BVdb publication page