Variant ID: 1-55519238-C-T

NM_174936.3(PCSK9):c.799+774C>T

This variant was identified in 1 publication



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

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: rs521662
PMID: 18300938
View BVdb publication page


Alternative transcript annotations:

Transcript cDNA Protein Consequence Exon Intron
ENST00000302118.5 c.799+774C>T - intron_variant - 5/11
ENST00000490692.1 n.1620+774C>T - intron_variant,non_coding_transcript_variant - 2/7
ENST00000543384.1 c.199+774C>T - intron_variant - 3/9
NM_174936.4 c.799+774C>T - intron_variant - 5/11
NR_110451.1 n.458+774C>T - intron_variant,non_coding_transcript_variant - 3/9