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RET c.577_579delinsATC ;(p.V193I)
Variant ID: 10-43598029-GTG-ATC
NM_020975.4(
RET
):c.577_579delinsATC;(p.V193I)
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:
Next-generation sequencing in thyroid cancers: do targetable alterations lead to a therapeutic advantage?: A multicenter experience.
Medicine
Moore, Assaf A; Bar, Yael Y; Maurice-Dror, Corinne C; Finkel, Inbar I; Goldvaser, Hadar H; Dudnik, Elizabeth E; Goldstein, Daniel A DA; Gordon, Noa N; Billan, Salem S; Gutfeld, Orit O; Wolf, Ido I; Popovtzer, Aron A
Publication Date: 2021-06-25
Variant appearance in text: RET: V193I
PubMed Link:
34160418
Variant Present in the following documents:
Main text
medi-100-e26388.pdf
View BVdb publication page