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TG c.5020C>A ;(p.P1674T)
Variant ID: 8-133948088-C-A
NM_003235.4(
TG
):c.5020C>A;(p.P1674T)
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:
Newborn Screening and Molecular Profile of Congenital Hypothyroidism in a Chinese Population.
Frontiers In Genetics
Yu, Bin B; Long, Wei W; Yang, Yuqi Y; Wang, Ying Y; Jiang, Lihua L; Cai, Zhengmao Z; Wang, Huaiyan H
Publication Date: 2018
Variant appearance in text: TG: 5020C>A; P1674T
PubMed Link:
30420871
Variant Present in the following documents:
Main text
fgene-09-00509.pdf
View BVdb publication page
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: TG: P1674T
PubMed Link:
27267998
Variant Present in the following documents:
supp_bgw066_Supplementary_File_1_151127.xlsx, sheet 4
View BVdb publication page