Bibliome.ai browser hg19
Search
About
Stats
FAQ
ERBB2 c.65G>T ;(p.S22I)
Variant ID: 17-37856556-G-T
NM_004448.2(
ERBB2
):c.65G>T;(p.S22I)
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:
Dynamic cfDNA Analysis by NGS in EGFR T790M-Positive Advanced NSCLC Patients Failed to the First-Generation EGFR-TKIs.
Frontiers In Oncology
Ma, Li L; Li, Haoyang H; Wang, Dongpo D; Hu, Ying Y; Yu, Mengjun M; Zhang, Quan Q; Qin, Na N; Zhang, Xinyong X; Li, Xi X; Zhang, Hui H; Wu, Yuhua Y; Lv, Jialin J; Yang, Xinjie X; Yu, Ruoying R; Zhang, Shucai S; Wang, Jinghui J
Publication Date: 2021
Variant appearance in text: ERBB2: S22I
PubMed Link:
33842353
Variant Present in the following documents:
Main text
fonc-11-643199.pdf
View BVdb publication page
Pan-urologic cancer genomic subtypes that transcend tissue of origin.
Nature Communications
Chen, Fengju F; Zhang, Yiqun Y; Bossé, Dominick D; Lalani, Aly-Khan A AA; Hakimi, A Ari AA; Hsieh, James J JJ; Choueiri, Toni K TK; Gibbons, Don L DL; Ittmann, Michael M; Creighton, Chad J CJ
Publication Date: 2017-08-04
Variant appearance in text: ERBB2: 65G>T
PubMed Link:
28775315
Variant Present in the following documents:
41467_2017_289_MOESM7_ESM.xlsx, sheet 1
View BVdb publication page