Variant ID: 1-55523209-T-C

NM_174936.3(PCSK9):c.1180+22T>C

This variant was identified in 1 publication




Publications:


Update of the Portuguese Familial Hypercholesterolaemia Study.

Atherosclerosis
AM Medeiros, AC Alves, V Francisco, M Bourbon,
Publication Date: 2010-10

Variant appearance in text: PCSK9: 1180+22T>C
PubMed Link: 20828696
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.1180+22T>C - intron_variant - 7/11
ENST00000490692.1 n.1904+22T>C - intron_variant,non_coding_transcript_variant - 4/7
ENST00000543384.1 c.580+22T>C - intron_variant - 5/9
NM_174936.4 c.1180+22T>C - intron_variant - 7/11
NR_110451.1 n.839+22T>C - intron_variant,non_coding_transcript_variant - 5/9