PRKCA c.918+871C>G

Variant ID: 17-64686036-C-G

NM_002737.2(PRKCA):c.918+871C>G

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Fine-scale haplotype mapping of MUT, AACS, SLC6A15 and PRKCA genes indicates association with insulin resistance of metabolic syndrome and relationship with branched chain amino acid metabolism or regulation.

Plos One
Haydar, Sara S; Grigorescu, Florin F; Vintilă, Mădălina M; Cogne, Yannick Y; Lautier, Corinne C; Tutuncu, Yildiz Y; Brun, Jean Frederic JF; Robine, Jean Marie JM; Pugeat, Michel M; Normand, Christophe C; Poucheret, Patrick P; Gheorghiu, Monica Livia ML; Georgescu, Carmen C; Badiu, Corin C; Băculescu, Nicoleta N; Renard, Eric E; Ylli, Dorina D; Badiou, Stephanie S; Sutra, Thibault T; Cristol, Jean Paul JP; Mercier, Jacques J; Gomis, Ramon R; Macias, Josep Maria JM; Litvinov, Serghey S; Khusnutdinova, Elza E; Poiana, Catalina C; Pasquali, Renato R; Lauro, Davide D; Sesti, Giorgio G; Prudente, Sabrina S; Trischitta, Vincenzo V; Tsatsoulis, Agathocles A; Abdelhak, Sonia S; Barakat, Abdelhamid A; Zenati, Akila A; Ylli, Agron A; Satman, Ilhan I; Kanninen, Timo T; Rinato, Yves Y; Missoni, Sasa S
Publication Date: 2019

Variant appearance in text: rs8072511
PubMed Link: 30913280
Variant Present in the following documents:
  • Main text
  • pone.0214122.pdf
View BVdb publication page



Whole genome sequencing identifies high-impact variants in well-known pharmacogenomic genes.

The Pharmacogenomics Journal
Choi, Jihoon J; Tantisira, Kelan G KG; Duan, Qing Ling QL
Publication Date: 2019-04

Variant appearance in text: rs8072511
PubMed Link: 30214008
Variant Present in the following documents:
  • NIHMS1503453-supplement-3.xlsx, sheet 1
View BVdb publication page