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SI c.646_647delinsTT ;(p.S216F)
Variant ID: 3-164783209-CT-AA
NM_001041.3(
SI
):c.646_647delinsTT;(p.S216F)
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:
Whole-exome sequencing of cervical carcinomas identifies activating ERBB2 and PIK3CA mutations as targets for combination therapy.
Proceedings Of The National Academy Of Sciences Of The United States Of America
Zammataro, Luca L; Lopez, Salvatore S; Bellone, Stefania S; Pettinella, Francesca F; Bonazzoli, Elena E; Perrone, Emanuele E; Zhao, Siming S; Menderes, Gulden G; Altwerger, Gary G; Han, Chanhee C; Zeybek, Burak B; Bianchi, Anna A; Manzano, Aranzazu A; Manara, Paola P; Cocco, Emiliano E; Buza, Natalia N; Hui, Pei P; Wong, Serena S; Ravaggi, Antonella A; Bignotti, Eliana E; Romani, Chiara C; Todeschini, Paola P; Zanotti, Laura L; Odicino, Franco F; Pecorelli, Sergio S; Donzelli, Carla C; Ardighieri, Laura L; Angioli, Roberto R; Raspagliesi, Francesco F; Scambia, Giovanni G; Choi, Jungmin J; Dong, Weilai W; Bilguvar, Kaya K; Alexandrov, Ludmil B LB; Silasi, Dan-Arin DA; Huang, Gloria S GS; Ratner, Elena E; Azodi, Masoud M; Schwartz, Peter E PE; Pirazzoli, Valentina V; Stiegler, Amy L AL; Boggon, Titus J TJ; Lifton, Richard P RP; Schlessinger, Joseph J; Santin, Alessandro D AD
Publication Date: 2019-11-05
Variant appearance in text: SI: S216F
PubMed Link:
31624127
Variant Present in the following documents:
Main text
View BVdb publication page