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CHRNB2 c.1067G>A ;(p.C356Y)
Variant ID: 1-154544366-G-A
NM_000748.2(
CHRNB2
):c.1067G>A;(p.C356Y)
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 mutational landscape of neuroendocrine carcinomas of the gallbladder.
Signal Transduction And Targeted Therapy
Liu, Fatao F; Li, Yongsheng Y; Ying, Dongjian D; Qiu, Shimei S; He, Yong Y; Li, Maolan M; Liu, Yun Y; Zhang, Yijian Y; Zhu, Qin Q; Hu, Yunping Y; Liu, Liguo L; Li, Guoqiang G; Pan, Weihua W; Jin, Wei W; Mu, Jiasheng J; Cao, Yang Y; Liu, Yingbin Y
Publication Date: 2021-02-10
Variant appearance in text: CHRNB2: Cys356Tyr
PubMed Link:
33563892
Variant Present in the following documents:
41392_2020_412_MOESM7_ESM.xlsx, sheet 1
View BVdb publication page