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BRAF c.1791_1792insACA ;(p.L597_A598insT)
Variant ID: 7-140453143-C-CTGT
NM_004333.4(
BRAF
):c.1791_1792insACA;(p.L597_A598insT)
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:
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: BRAF: L597_A598insT
PubMed Link:
36906579
Variant Present in the following documents:
41467_2023_36922_MOESM4_ESM.xls, sheet 2
View BVdb publication page