PROCR c.472T>C ;(p.S158P)

Variant ID: 20-33764120-T-C

NM_006404.4(PROCR):c.472T>C;(p.S158P)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Thrombophilia in East Asian countries: are there any genetic differences in these countries?

Thrombosis Journal
Miyata, Toshiyuki T; Maruyama, Keiko K; Banno, Fumiaki F; Neki, Reiko R
Publication Date: 2016

Variant appearance in text: EPCR: S158P
PubMed Link: 27766051
Variant Present in the following documents:
  • Main text
  • 12959_2016_Article_109.pdf
View BVdb publication page



The eSNV-detect: a computational system to identify expressed single nucleotide variants from transcriptome sequencing data.

Nucleic Acids Research
Tang, Xiaojia X; Baheti, Saurabh S; Shameer, Khader K; Thompson, Kevin J KJ; Wills, Quin Q; Niu, Nifang N; Holcomb, Ilona N IN; Boutet, Stephane C SC; Ramakrishnan, Ramesh R; Kachergus, Jennifer M JM; Kocher, Jean-Pierre A JP; Weinshilboum, Richard M RM; Wang, Liewei L; Thompson, E Aubrey EA; Kalari, Krishna R KR
Publication Date: 2014-12-16

Variant appearance in text: PROCR: S158P
PubMed Link: 25352556
Variant Present in the following documents:
  • supp_gku1005_nar-01266-met-n-2014-File014.xlsx, sheet 10
View BVdb publication page