Variant ID: 1-55527217-C-T

NM_174936.3(PCSK9):c.1851C>T;(p.Ala617Ala)

This variant was identified in 1 publication




Publications:


PCSK9 variation and association with blood pressure in African Americans: preliminary findings from the HyperGEN and REGARDS studies.

Frontiers In Genetics
NT Tran, S Aslibekyan, HK Tiwari, D Zhi, YJ Sung, SC Hunt, DC Rao, U Broeckel, SE Judd, P Muntner, ST Kent, DK Arnett, MR Irvin
Publication Date: 2015

Variant appearance in text: PCSK9: A617A; rs140364657
PMID: 25904937
View BVdb publication page



Alternative transcript annotations:

Transcript cDNA Protein Consequence Exon Intron
ENST00000302118.5 c.1851C>T p.Ala617= synonymous_variant 11/12 -
ENST00000490692.1 n.2397C>T - non_coding_transcript_exon_variant 7/8 -
ENST00000543384.1 c.*398C>T - 3_prime_UTR_variant 9/10 -
NM_174936.4 c.1851C>T p.Ala617= synonymous_variant 11/12 -
NR_110451.1 n.1458C>T - non_coding_transcript_exon_variant 9/10 -