Variant ID: 1-55518166-G-C

NM_174936.3(PCSK9):c.657+82G>C

This variant was identified in 1 publication




Publications:


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: rs625619
PMID: 18300938
View BVdb publication page



Alternative transcript annotations:

Transcript cDNA Protein Consequence Exon Intron
ENST00000302118.5 c.657+82G>C - intron_variant - 4/11
ENST00000452118.2 c.*301+82G>C - intron_variant - 5/5
ENST00000490692.1 n.1478+82G>C - intron_variant,non_coding_transcript_variant - 1/7
ENST00000543384.1 c.57+82G>C - intron_variant - 2/9
NM_174936.4 c.657+82G>C - intron_variant - 4/11
NR_110451.1 n.316+82G>C - intron_variant,non_coding_transcript_variant - 2/9