Variant ID: 1-55518287-G-A

NM_174936.3(PCSK9):c.658-36G>A

This variant was identified in 1 publication



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

Publications:

A new PCSK9 gene promoter variant affects gene expression and causes autosomal dominant hypercholesterolemia.

The Journal Of Clinical Endocrinology And Metabolism
S Blesa, S Vernia, AB Garcia-Garcia, S Martinez-Hervas, C Ivorra, V Gonzalez-Albert, JF Ascaso, JC Martín-Escudero, JT Real, R Carmena, M Casado, FJ Chaves
Publication Date: 2008-09

Variant appearance in text: rs11800265
PubMed Link: 18559913
Variant Present in the following documents:
  • Supplemental file
  • Main text
View BVdb publication page


Alternative transcript annotations:

Transcript cDNA Protein Consequence Exon Intron
ENST00000302118.5 c.658-36G>A - intron_variant - 4/11
ENST00000452118.2 c.*302-36G>A - intron_variant - 5/5
ENST00000490692.1 n.1479-36G>A - intron_variant,non_coding_transcript_variant - 1/7
ENST00000543384.1 c.58-36G>A - intron_variant - 2/9
NM_174936.4 c.658-36G>A - intron_variant - 4/11
NR_110451.1 n.317-36G>A - intron_variant,non_coding_transcript_variant - 2/9