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RET c.3151G>A ;(p.A1051T)
Variant ID: 10-43622134-G-A
NM_020975.4(
RET
):c.3151G>A;(p.A1051T)
This variant was identified in 3 publications
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
Publications:
Comprehensive germline and somatic genomic profiles of Chinese patients with biliary tract cancer.
Frontiers In Oncology
Yu, Haipeng H; Xu, Yan Y; Gao, Wei W; Li, Mei M; He, Ji'an J; Deng, Xiaoqian X; Xing, Wenge W
Publication Date: 2022
Variant appearance in text: RET: A1051T
PubMed Link:
36072793
Variant Present in the following documents:
Table_3.xlsx, sheet 1
View BVdb publication page
A full-proteome, interaction-specific characterization of mutational hotspots across human cancers.
Genome Research
Chen, Siwei S; Liu, Yuan Y; Zhang, Yingying Y; Wierbowski, Shayne D SD; Lipkin, Steven M SM; Wei, Xiaomu X; Yu, Haiyuan H
Publication Date: 2022-01
Variant appearance in text: RET: A1051T
PubMed Link:
34963661
Variant Present in the following documents:
supp_gr.275437.121_Supplementary_Table_1.xlsx, sheet 3
View BVdb publication page
Kinome sequencing reveals RET G691S polymorphism in human neuroendocrine lung cancer cell lines.
Genes & Genomics
Sosonkina, Nadiya N; Hong, Seung-Keun SK; Starenki, Dmytro D; Park, Jong-In JI
Publication Date: 2014-12
Variant appearance in text: RET: 3151G>A
PubMed Link:
25530832
Variant Present in the following documents:
Main text
View BVdb publication page