Bibliome.ai browser hg19
Search
About
Stats
FAQ
KRT2 c.1650C>T ;(p.G550=)
Variant ID: 12-53039073-G-A
NM_000423.2(
KRT2
):c.1650C>T;(p.G550=)
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:
Evolving neoantigen profiles in colorectal cancers with DNA repair defects.
Genome Medicine
Rospo, Giuseppe G; Lorenzato, Annalisa A; Amirouchene-Angelozzi, Nabil N; Magrì, Alessandro A; Cancelliere, Carlotta C; Corti, Giorgio G; Negrino, Carola C; Amodio, Vito V; Montone, Monica M; Bartolini, Alice A; Barault, Ludovic L; Novara, Luca L; Isella, Claudio C; Medico, Enzo E; Bertotti, Andrea A; Trusolino, Livio L; Germano, Giovanni G; Di Nicolantonio, Federica F; Bardelli, Alberto A
Publication Date: 2019-06-28
Variant appearance in text: KRT2: G550G
PubMed Link:
31253177
Variant Present in the following documents:
13073_2019_654_MOESM2_ESM.xlsx, sheet 63
View BVdb publication page
Genomic regions identified by overlapping clusters of nominally-positive SNPs from genome-wide studies of alcohol and illegal substance dependence.
Plos One
Johnson, Catherine C; Drgon, Tomas T; Walther, Donna D; Uhl, George R GR
Publication Date: 2011
Variant appearance in text: rs2232562
PubMed Link:
21818250
Variant Present in the following documents:
Main text
View BVdb publication page