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RET c.2552_2553delinsAA ;(p.L851Q)
Variant ID: 10-43615138-TC-AA
NM_020975.4(
RET
):c.2552_2553delinsAA;(p.L851Q)
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:
Clinical Utility of Liquid Biopsy-Based Actionable Mutations Detected via ddPCR.
Biomedicines
Palacín-Aliana, Irina I; García-Romero, Noemí N; Asensi-Puig, Adrià A; Carrión-Navarro, Josefa J; González-Rumayor, Víctor V; Ayuso-Sacido, Ángel Á
Publication Date: 2021-07-28
Variant appearance in text: RET: L851Q
PubMed Link:
34440110
Variant Present in the following documents:
Main text
biomedicines-09-00906.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: L851Q
PubMed Link:
31819097
Variant Present in the following documents:
41598_2019_54976_MOESM2_ESM.xlsx, sheet 8
View BVdb publication page