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RET c.2302G>A ;(p.E768K)
Variant ID: 10-43613838-G-A
NM_020975.4(
RET
):c.2302G>A;(p.E768K)
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:
The Mutational Landscape of Early-Onset Breast Cancer: A Next-Generation Sequencing Analysis.
Frontiers In Oncology
Andrikopoulou, Angeliki A; Chatzinikolaou, Spyridoula S; Kyriopoulos, Ilias I; Bletsa, Garyfalia G; Kaparelou, Maria M; Liontos, Michalis M; Dimopoulos, Meletios-Athanasios MA; Zagouri, Flora F
Publication Date: 2021
Variant appearance in text: RET: 2302G>A; Glu768Lys
PubMed Link:
35127508
Variant Present in the following documents:
Main text
fonc-11-797505.pdf
View BVdb publication page
TP53 mutations determined by targeted NGS in breast cancer: a case-control study.
Oncotarget
Andrikopoulou, Angeliki A; Terpos, Evangelos E; Chatzinikolaou, Spyridoula S; Apostolidou, Kleoniki K; Ntanasis-Stathopoulos, Ioannis I; Gavriatopoulou, Maria M; Dimopoulos, Meletios-Athanasios MA; Zagouri, Flora F
Publication Date: 2021-10-12
Variant appearance in text: RET: Glu768Lys
PubMed Link:
34676052
Variant Present in the following documents:
Main text
oncotarget-12-2206.pdf
View BVdb publication page
Refinement of evolutionary medicine predictions based on clinical evidence for the manifestations of Mendelian diseases.
Scientific Reports
Šimčíková, Daniela D; Heneberg, Petr P
Publication Date: 2019-12-09
Variant appearance in text: RET: E768K
PubMed Link:
31819097
Variant Present in the following documents:
41598_2019_54976_MOESM2_ESM.xlsx, sheet 8
View BVdb publication page