Bibliome.ai browser hg19
Search
About
Stats
FAQ
ERBB2 c.2653C>T ;(p.P885S)
Variant ID: 17-37881583-C-T
NM_004448.2(
ERBB2
):c.2653C>T;(p.P885S)
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:
Finding driver mutations in cancer: Elucidating the role of background mutational processes.
Plos Computational Biology
Brown, Anna-Leigh AL; Li, Minghui M; Goncearenco, Alexander A; Panchenko, Anna R AR
Publication Date: 2019-04
Variant appearance in text: ERBB2: P885S
PubMed Link:
31034466
Variant Present in the following documents:
pcbi.1006981.s010.xlsx, sheet 1
View BVdb publication page
HER2 somatic mutations are associated with poor survival in HER2-negative breast cancers.
Cancer Science
Wang, Tonghui T; Xu, Ye Y; Sheng, Shuyan S; Yuan, Hua H; Ouyang, Tao T; Li, Jinfeng J; Wang, Tianfeng T; Fan, Zhaoqing Z; Fan, Tie T; Lin, Benyao B; Xie, Yuntao Y
Publication Date: 2017-04
Variant appearance in text: HER2: P885S
PubMed Link:
28164408
Variant Present in the following documents:
Main text
CAS-108-671.pdf
View BVdb publication page