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PC c.466_468del ;(p.R156del)
Variant ID: 11-66638805-CCCG-C
NM_001040716.1(
PC
):c.466_468del;(p.R156del)
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:
Molecular spectrum of TP53 mutations in plasma cell dyscrasias by next generation sequencing: an Italian cohort study and overview of the literature.
Oncotarget
Lionetti, Marta M; Barbieri, Marzia M; Manzoni, Martina M; Fabris, Sonia S; Bandini, Cecilia C; Todoerti, Katia K; Nozza, Filomena F; Rossi, Davide D; Musto, Pellegrino P; Baldini, Luca L; Neri, Antonino A
Publication Date: 2016-04-19
Variant appearance in text: PC: R156del
PubMed Link:
26870891
Variant Present in the following documents:
Main text
oncotarget-07-21353.pdf
View BVdb publication page