Variant ID: 1-55529602-C-T

NM_174936.3(PCSK9):c.*345C>T

This variant was identified in 2 publications




Publications:


Lipid lowering and Alzheimer disease risk: A mendelian randomization study.

Annals Of Neurology
DM Williams, C Finan, AF Schmidt, S Burgess, AD Hingorani
Publication Date: 2020-01

Variant appearance in text: rs17111555
PubMed Link: 31714636
Variant Present in the following documents:
  • ANA-87-30-s001.docx
View BVdb publication page



Next-generation-sequencing-based identification of familial hypercholesterolemia-related mutations in subjects with increased LDL-C levels in a latvian population.

Bmc Medical Genetics
I Radovica-Spalvina, G Latkovskis, I Silamikelis, D Fridmanis, I Elbere, K Ventins, G Ozola, A Erglis, J Klovins
Publication Date: 2015-09-28

Variant appearance in text: rs17111555
PubMed Link: 26415676
Variant Present in the following documents:
  • 12881_2015_230_MOESM1_ESM.doc
View BVdb publication page



Alternative transcript annotations:

Transcript cDNA Protein Consequence Exon Intron
ENST00000302118.5 c.*345C>T - 3_prime_UTR_variant 12/12 -
ENST00000490692.1 n.2970C>T - non_coding_transcript_exon_variant 8/8 -
NM_174936.4 c.*345C>T - 3_prime_UTR_variant 12/12 -
NR_110451.1 n.2031C>T - non_coding_transcript_exon_variant 10/10 -