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TP53 c.927C>G ;(p.P309=)
Variant ID: 17-7576919-G-C
NM_000546.5(
TP53
):c.927C>G;(p.P309=)
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:
Different hotspot p53 mutants exert distinct phenotypes and predict outcome of colorectal cancer patients.
Nature Communications
Hassin, Ori O; Nataraj, Nishanth Belugali NB; Shreberk-Shaked, Michal M; Aylon, Yael Y; Yaeger, Rona R; Fontemaggi, Giulia G; Mukherjee, Saptaparna S; Maddalena, Martino M; Avioz, Adi A; Iancu, Ortal O; Mallel, Giuseppe G; Gershoni, Anat A; Grosheva, Inna I; Feldmesser, Ester E; Ben-Dor, Shifra S; Golani, Ofra O; Hendel, Ayal A; Blandino, Giovanni G; Kelsen, David D; Yarden, Yosef Y; Oren, Moshe M
Publication Date: 2022-05-19
Variant appearance in text: p53: P309P
PubMed Link:
35589715
Variant Present in the following documents:
Main text
View BVdb publication page
Germ-line and somatic EPHA2 coding variants in lens aging and cataract.
Plos One
Bennett, Thomas M TM; M'Hamdi, Oussama O; Hejtmancik, J Fielding JF; Shiels, Alan A
Publication Date: 2017
Variant appearance in text: TP53: P309P
PubMed Link:
29267365
Variant Present in the following documents:
pone.0189881.s008.xlsx, sheet 1
View BVdb publication page