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RARA c.837C>A ;(p.P279=)
Variant ID: 17-38510583-C-A
NM_000964.3(
RARA
):c.837C>A;(p.P279=)
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:
Molecular networks of hepatoblastoma predisposition and oncogenesis in Beckwith-Wiedemann syndrome.
Hepatology Communications
Sobel Naveh, Natali S NS; Traxler, Emily M EM; Duffy, Kelly A KA; Kalish, Jennifer M JM
Publication Date: 2022-08
Variant appearance in text: RARA: P279P; rs77633370
PubMed Link:
35507738
Variant Present in the following documents:
HEP4-6-2132-s005.xlsx, sheet 1
View BVdb publication page
Cas9 activates the p53 pathway and selects for p53-inactivating mutations.
Nature Genetics
Enache, Oana M OM; Rendo, Veronica V; Abdusamad, Mai M; Lam, Daniel D; Davison, Desiree D; Pal, Sangita S; Currimjee, Naomi N; Hess, Julian J; Pantel, Sasha S; Nag, Anwesha A; Thorner, Aaron R AR; Doench, John G JG; Vazquez, Francisca F; Beroukhim, Rameen R; Golub, Todd R TR; Ben-David, Uri U
Publication Date: 2020-07
Variant appearance in text: RARA: P279P; rs77633370
PubMed Link:
32424350
Variant Present in the following documents:
NIHMS1581982-supplement-1581982_Supp_Dataset1-7.xlsx, sheet 7
View BVdb publication page