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HR c.1495_1496delinsTT ;(p.S499F)
Variant ID: 8-21983155-CT-AA
NM_005144.4(
HR
):c.1495_1496delinsTT;(p.S499F)
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:
Mutational Landscape of PI3K-AKT-mTOR Pathway in Breast Cancer: Implications for Targeted Therapeutics.
Journal Of Cancer
Xiao, Weikai W; Zhang, Guochun G; Chen, Bo B; Chen, Xiaoqing X; Wen, Lingzhu L; Lai, Jianguo J; Li, Xuerui X; Li, Min M; Liu, Hao H; Liu, Jing J; Han-Zhang, Han H; Lizaso, Analyn A; Liao, Ning N
Publication Date: 2021
Variant appearance in text: HR: S499F
PubMed Link:
34093841
Variant Present in the following documents:
Main text
jcav12p4408.pdf
View BVdb publication page
Genetic mutation profile of Chinese HER2-positive breast cancers and genetic predictors of responses to Neoadjuvant anti-HER2 therapy.
Breast Cancer Research And Treatment
Li, Kai K; Liao, Ning N; Chen, Bo B; Zhang, Guochun G; Wang, Yulei Y; Guo, Liping L; Wei, Guangnan G; Jia, Minghan M; Wen, Lingzhu L; Ren, Chongyang C; Cao, Li L; Mok, Hsiaopei H; Li, Cheukfai C; Lin, Jiali J; Chen, Xiaoqing X; Zhang, Zhou Z; Hou, Ting T; Li, Min M; Liu, Jing J; Balch, Charles M CM; Liao, Ning N
Publication Date: 2020-09
Variant appearance in text: HR: S499F
PubMed Link:
32638235
Variant Present in the following documents:
10549_2020_Article_5778.pdf
View BVdb publication page