NR0B2 c.112C>T ;(p.R38C)

Variant ID: 1-27240320-G-A

NM_021969.2(NR0B2):c.112C>T;(p.R38C)

This variant was identified in 3 publications

View GRCh38 version.




Publications:


Evolving neoantigen profiles in colorectal cancers with DNA repair defects.

Genome Medicine
Rospo, Giuseppe G; Lorenzato, Annalisa A; Amirouchene-Angelozzi, Nabil N; Magrì, Alessandro A; Cancelliere, Carlotta C; Corti, Giorgio G; Negrino, Carola C; Amodio, Vito V; Montone, Monica M; Bartolini, Alice A; Barault, Ludovic L; Novara, Luca L; Isella, Claudio C; Medico, Enzo E; Bertotti, Andrea A; Trusolino, Livio L; Germano, Giovanni G; Di Nicolantonio, Federica F; Bardelli, Alberto A
Publication Date: 2019-06-28

Variant appearance in text: NR0B2: R38C
PubMed Link: 31253177
Variant Present in the following documents:
  • 13073_2019_654_MOESM2_ESM.xlsx, sheet 32
View BVdb publication page



Role of nuclear receptor SHP in metabolism and cancer.

Biochimica Et Biophysica Acta
Zhang, Yuxia Y; Hagedorn, Curt H CH; Wang, Li L
Publication Date: 2011-08

Variant appearance in text: SHP: 112C>T
PubMed Link: 20970497
Variant Present in the following documents:
  • Main text
View BVdb publication page



Novel polymorphisms of nuclear receptor SHP associated with functional and structural changes.

The Journal Of Biological Chemistry
Zhou, Taofeng T; Zhang, Yuxia Y; Macchiarulo, Antonio A; Yang, Zhihong Z; Cellanetti, Marco M; Coto, Eliecer E; Xu, Pingyi P; Pellicciari, Roberto R; Wang, Li L
Publication Date: 2010-08-06

Variant appearance in text: SHP: R38C
PubMed Link: 20516075
Variant Present in the following documents:
  • Main text
View BVdb publication page