Variant ID: 1-55527918-C-T

NM_174936.3(PCSK9):c.1863+689C>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: rs643257
PMID: 18300938
View BVdb publication page


Alternative transcript annotations:

Transcript cDNA Protein Consequence Exon Intron
ENST00000302118.5 c.1863+689C>T - intron_variant - 11/11
ENST00000490692.1 n.2409+689C>T - intron_variant,non_coding_transcript_variant - 7/7
ENST00000543384.1 c.*410+689C>T - intron_variant - 9/9
NM_174936.4 c.1863+689C>T - intron_variant - 11/11
NR_110451.1 n.1470+689C>T - intron_variant,non_coding_transcript_variant - 9/9