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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.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
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