Bibliome.ai browser hg19
Search
About
Stats
FAQ
BRAF c.1405_1406delinsTC ;(p.G469S)
Variant ID: 7-140481402-CC-GA
NM_004333.4(
BRAF
):c.1405_1406delinsTC;(p.G469S)
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:
Usefulness of a novel device to divide core needle biopsy specimens in a spatially matched fashion.
Scientific Reports
Shiraishi, Takumi T; Inui, Shogo S; Inoue, Yuta Y; Saito, Yumiko Y; Taga, Hideto H; Kaneko, Masatomo M; Tsuji, Keisuke K; Ueda, Saya S; Ueda, Takashi T; Matsugasumi, Toru T; Taniguchi, Hidefumi H; Ueno, Akihisa A; Yamada, Takeshi T; Yamada, Yasuhiro Y; Iwata, Tsuyoshi T; Fujihara, Atsuko A; Hongo, Fumiya F; Ukimura, Osamu O
Publication Date: 2020-10-13
Variant appearance in text: rs1057519720
PubMed Link:
33051506
Variant Present in the following documents:
41598_2020_74136_MOESM2_ESM.xlsx, sheet 1
View BVdb publication page
Identification of pathogenic missense mutations using protein stability predictors.
Scientific Reports
Gerasimavicius, Lukas L; Liu, Xin X; Marsh, Joseph A JA
Publication Date: 2020-09-21
Variant appearance in text: N/A
PubMed Link:
32958805
Variant Present in the following documents:
View BVdb publication page