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RET c.1921G>T ;(p.A641S)
Variant ID: 10-43609969-G-T
NM_020975.4(
RET
):c.1921G>T;(p.A641S)
This variant was identified in 6 publications
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
Publications:
Predictive mutation signature of immunotherapy benefits in NSCLC based on machine learning algorithms.
Frontiers In Immunology
Liu, Zhichao Z; Lin, Guo G; Yan, Zeping Z; Li, Linduo L; Wu, Xingchen X; Shi, Jingrong J; He, Jianxing J; Zhao, Lei L; Liang, Hengrui H; Wang, Wei W
Publication Date: 2022
Variant appearance in text: RET: 1921G>T; A641S
PubMed Link:
36238300
Variant Present in the following documents:
Table_1.xlsx, sheet 4
View BVdb publication page
EPHA5 mutation was associated with adverse outcome of atezolizumab treatment in late-stage non-small cell lung cancers.
Bmc Pulmonary Medicine
Li, Zhenxiang Z; Zhou, Qing Q; Wang, Qi Q; Wang, Haiyong H; Yue, Weiming W
Publication Date: 2022-09-19
Variant appearance in text: RET: 1921G>T; A641S
PubMed Link:
36123678
Variant Present in the following documents:
12890_2022_2161_MOESM2_ESM.xlsx, sheet 1
View BVdb publication page
TAPES: A tool for assessment and prioritisation in exome studies.
Plos Computational Biology
Xavier, Alexandre A; Scott, Rodney J RJ; Talseth-Palmer, Bente A BA
Publication Date: 2019-10
Variant appearance in text: RET: A641S; rs377767411
PubMed Link:
31613886
Variant Present in the following documents:
pcbi.1007453.s004.xlsx, sheet 7
pcbi.1007453.s002.xlsx, sheet 1
pcbi.1007453.s004.xlsx, sheet 2
pcbi.1007453.s004.xlsx, sheet 6
View BVdb publication page
Absence of BRAF mutation in pheochromocytoma and paraganglioma.
Neoplasma
Vosecka, T T; Vicha, A A; Zelinka, T T; Jencova, P P; Pacak, K K; Duskova, J J; Benes, J J; Guha, A A; Stanek, L L; Kohoutova, M M; Musil, Z Z
Publication Date: 2017
Variant appearance in text: RET: 1921G>T; Ala641Ser
PubMed Link:
28043156
Variant Present in the following documents:
Main text
View BVdb publication page
Exome sequencing of hepatocellular carcinomas identifies new mutational signatures and potential therapeutic targets.
Nature Genetics
Schulze, Kornelius K; Imbeaud, Sandrine S; Letouzé, Eric E; Alexandrov, Ludmil B LB; Calderaro, Julien J; Rebouissou, Sandra S; Couchy, Gabrielle G; Meiller, Clément C; Shinde, Jayendra J; Soysouvanh, Frederic F; Calatayud, Anna-Line AL; Pinyol, Roser R; Pelletier, Laura L; Balabaud, Charles C; Laurent, Alexis A; Blanc, Jean-Frederic JF; Mazzaferro, Vincenzo V; Calvo, Fabien F; Villanueva, Augusto A; Nault, Jean-Charles JC; Bioulac-Sage, Paulette P; Stratton, Michael R MR; Llovet, Josep M JM; Zucman-Rossi, Jessica J
Publication Date: 2015-05
Variant appearance in text: RET: A641S
PubMed Link:
25822088
Variant Present in the following documents:
NIHMS62359-supplement-Table3.xlsx, sheet 1
View BVdb publication page
RET germline mutations identified by exome sequencing in a Chinese multiple endocrine neoplasia type 2A/familial medullary thyroid carcinoma family.
Plos One
Qi, Xiao-Ping XP; Ma, Ju-Ming JM; Du, Zhen-Fang ZF; Ying, Rong-Biao RB; Fei, Jun J; Jin, Hang-Yang HY; Han, Jian-Shan JS; Wang, Jin-Quan JQ; Chen, Xiao-Ling XL; Chen, Chun-Yue CY; Liu, Wen-Ting WT; Lu, Jia-Jun JJ; Zhang, Jian-Guo JG; Zhang, Xian-Ning XN
Publication Date: 2011
Variant appearance in text: RET: A641S
PubMed Link:
21655256
Variant Present in the following documents:
Main text
pone.0020353.pdf
View BVdb publication page