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.




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