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GCNT2 c.34_35delinsCA ;(p.A12Q)
Variant ID: 6-10529178-GC-CA
NM_145649.4(
GCNT2
):c.34_35delinsCA;(p.A12Q)
This variant was identified in 2 publications
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
Publications:
Mutation Clusters from Cancer Exome.
Genes
Kakushadze, Zura Z; Yu, Willie W
Publication Date: 2017-08-15
Variant appearance in text: CCAT: A12Q
PubMed Link:
28809811
Variant Present in the following documents:
Main text
View BVdb publication page
Splicing mutation analysis reveals previously unrecognized pathways in lymph node-invasive breast cancer.
Scientific Reports
Dorman, Stephanie N SN; Viner, Coby C; Rogan, Peter K PK
Publication Date: 2014-11-14
Variant appearance in text: GCNT2: A12Q
PubMed Link:
25394353
Variant Present in the following documents:
srep07063-s2.xls, sheet 2
View BVdb publication page