Variant ID: 1-55518622-T-C

NM_174936.3(PCSK9):c.799+158T>C

This variant was identified in 1 publication




Publications:


Genetic associations between serum low LDL-cholesterol levels and variants in LDLR, APOB, PCSK9 and LDLRAP1 in African populations.

Plos One
M Hayat, R Kerr, AR Bentley, CN Rotimi, FJ Raal, M Ramsay
Publication Date: 2020

Variant appearance in text: rs45613943
PMID: 32084179
View BVdb publication page



Alternative transcript annotations:

Transcript cDNA Protein Consequence Exon Intron
ENST00000302118.5 c.799+158T>C - intron_variant - 5/11
ENST00000490692.1 n.1620+158T>C - intron_variant,non_coding_transcript_variant - 2/7
ENST00000543384.1 c.199+158T>C - intron_variant - 3/9
NM_174936.4 c.799+158T>C - intron_variant - 5/11
NR_110451.1 n.458+158T>C - intron_variant,non_coding_transcript_variant - 3/9