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RET c.1777_1779delinsTGT ;(p.G593C)
Variant ID: 10-43609021-GGA-TGT
NM_020975.4(
RET
):c.1777_1779delinsTGT;(p.G593C)
This variant was identified in 1 publication
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
Publications:
Inherited Thyroid Tumors With Oncocytic Change.
Frontiers In Endocrinology
Correia, Marcelo M; Lima, Ana Rita AR; Batista, Rui R; Máximo, Valdemar V; Sobrinho-Simões, Manuel M
Publication Date: 2021
Variant appearance in text: RET: G593C
PubMed Link:
34177813
Variant Present in the following documents:
Main text
fendo-12-691979.pdf
View BVdb publication page