Variant ID: 1-55526428-T-C

NM_174936.3(PCSK9):c.1682-620T>C

This variant was identified in 3 publications




Publications:


Association between the DOCK7, PCSK9 and GALNT2 Gene Polymorphisms and Serum Lipid levels.

Scientific Reports
T Guo, RX Yin, F Huang, LM Yao, WX Lin, SL Pan
Publication Date: 2016-01-08

Variant appearance in text: rs11206517
PMID: 26744084
View BVdb publication page



Association of the variants and haplotypes in the DOCK7, PCSK9 and GALNT2 genes and the risk of hyperlipidaemia.

Journal Of Cellular And Molecular Medicine
T Guo, RX Yin, WX Lin, W Wang, F Huang, SL Pan
Publication Date: 2016-02

Variant appearance in text: rs11206517
PMID: 26493351
View BVdb publication page



Molecular population genetics of PCSK9: a signature of recent positive selection.

Pharmacogenetics And Genomics
K Ding, IJ Kullo
Publication Date: 2008-03

Variant appearance in text: rs11206517
PMID: 18300938
View BVdb publication page



Alternative transcript annotations:

Transcript cDNA Protein Consequence Exon Intron
ENST00000302118.5 c.1682-620T>C - intron_variant - 10/11
ENST00000490692.1 n.2228-620T>C - intron_variant,non_coding_transcript_variant - 6/7
ENST00000543384.1 c.*229-620T>C - intron_variant - 8/9
NM_174936.4 c.1682-620T>C - intron_variant - 10/11
NR_110451.1 n.1289-620T>C - intron_variant,non_coding_transcript_variant - 8/9