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TNFRSF11A c.1239G>A ;(p.W413*)
Variant ID: 18-60036389-G-A
NM_003839.3(
TNFRSF11A
):c.1239G>A;(p.W413*)
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:
Hypermutation and unique mutational signatures of occupational cholangiocarcinoma in printing workers exposed to haloalkanes.
Carcinogenesis
Mimaki, Sachiyo S; Totsuka, Yukari Y; Suzuki, Yutaka Y; Nakai, Chikako C; Goto, Masanori M; Kojima, Motohiro M; Arakawa, Hirofumi H; Takemura, Shigekazu S; Tanaka, Shogo S; Marubashi, Shigeru S; Kinoshita, Masahiko M; Matsuda, Tomonari T; Shibata, Tatsuhiro T; Nakagama, Hitoshi H; Ochiai, Atsushi A; Kubo, Shoji S; Nakamori, Shoji S; Esumi, Hiroyasu H; Tsuchihara, Katsuya K
Publication Date: 2016-08
Variant appearance in text: TNFRSF11A: W413*
PubMed Link:
27267998
Variant Present in the following documents:
supp_bgw066_Supplementary_File_1_151127.xlsx, sheet 2
View BVdb publication page