PRKCA c.288+33994A>C

Variant ID: 17-64526395-A-C

NM_002737.2(PRKCA):c.288+33994A>C

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Inherited variations in human pigmentation-related genes modulate cutaneous melanoma risk and clinicopathological features in Brazilian population.

Scientific Reports
Lourenço, Gustavo Jacob GJ; Oliveira, Cristiane C; Carvalho, Benilton Sá BS; Torricelli, Caroline C; Silva, Janet Keller JK; Gomez, Gabriela Vilas Bôas GVB; Rinck-Junior, José Augusto JA; Oliveira, Wesley Lima WL; Vazquez, Vinicius Lima VL; Serrano, Sergio Vicente SV; Moraes, Aparecida Machado AM; Lima, Carmen Silvia Passos CSP
Publication Date: 2020-07-22

Variant appearance in text: rs1806448
PubMed Link: 32699307
Variant Present in the following documents:
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: rs1806448
PubMed Link: 30214008
Variant Present in the following documents:
  • NIHMS1503453-supplement-3.xlsx, sheet 1
View BVdb publication page