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ADRA2B c.632G>T ;(p.G211V)
Variant ID: 2-96781257-C-A
NM_000682.5(
ADRA2B
):c.632G>T;(p.G211V)
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:
Recapitulating thyroid cancer histotypes through engineering embryonic stem cells.
Nature Communications
Veschi, Veronica V; Turdo, Alice A; Modica, Chiara C; Verona, Francesco F; Di Franco, Simone S; Gaggianesi, Miriam M; TirrĂ², Elena E; Di Bella, Sebastiano S; Iacono, Melania Lo ML; Pantina, Vincenzo Davide VD; Porcelli, Gaetana G; Mangiapane, Laura Rosa LR; Bianca, Paola P; Rizzo, Aroldo A; Sciacca, Elisabetta E; Pillitteri, Irene I; Vella, Veronica V; Belfiore, Antonino A; Bongiorno, Maria Rita MR; Pistone, Giuseppe G; Memeo, Lorenzo L; Colarossi, Lorenzo L; Giuffrida, Dario D; Colarossi, Cristina C; Vigneri, Paolo P; Todaro, Matilde M; Stassi, Giorgio G
Publication Date: 2023-03-11
Variant appearance in text: rs9333568
PubMed Link:
36906579
Variant Present in the following documents:
41467_2023_36922_MOESM4_ESM.xls, sheet 2
View BVdb publication page
Parental segregation study reveals rare benign and likely benign variants in a Brazilian cohort of rare diseases.
Scientific Reports
Quaio, Caio Robledo D 'Angioli Costa CRD'C; Ceroni, Jose Ricardo Magliocco JRM; Cervato, Murilo Castro MC; Thurow, Helena Strelow HS; Moreira, Caroline Monaco CM; Trindade, Ana Carolina Gomes ACG; Furuzawa, Cintia Reys CR; de Souza, Rafaela Rogerio Floriano RRF; Perazzio, Sandro Felix SF; Dutra, Aurelio Pimenta AP; Chung, Christine Hsiaoyun CH; Kim, Chong Ae CA
Publication Date: 2022-05-11
Variant appearance in text: ADRA2B: 632G>T; Gly211Val; rs9333568
PubMed Link:
35546177
Variant Present in the following documents:
41598_2022_11932_MOESM1_ESM.xlsx, sheet 2
View BVdb publication page