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RET c.529_531delinsAGC ;(p.R177S)
Variant ID: 10-43597981-CGG-AGC
NM_020975.4(
RET
):c.529_531delinsAGC;(p.R177S)
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:
The paradox of cancer genes in non-malignant conditions: implications for precision medicine.
Genome Medicine
Adashek, Jacob J JJ; Kato, Shumei S; Lippman, Scott M SM; Kurzrock, Razelle R
Publication Date: 2020-02-17
Variant appearance in text: RET: R177S
PubMed Link:
32066498
Variant Present in the following documents:
Main text
13073_2020_Article_714.pdf
View BVdb publication page