Variant ID: 1-55527186-A-G

NM_174936.3(PCSK9):c.1820A>G;(p.Glu607Gly)

This variant was identified in 1 publication




Publications:


The genetics of ischaemic stroke.

Journal Of Internal Medicine
M Matarin, A Singleton, J Hardy, J Meschia
Publication Date: 2010-02

Variant appearance in text: PCSK9: E607G
PMID: 20175863
View BVdb publication page



Alternative transcript annotations:

Transcript cDNA Protein Consequence Exon Intron
ENST00000302118.5 c.1820A>G p.Glu607Gly missense_variant 11/12 -
ENST00000490692.1 n.2366A>G - non_coding_transcript_exon_variant 7/8 -
ENST00000543384.1 c.*367A>G - 3_prime_UTR_variant 9/10 -
NM_174936.4 c.1820A>G p.Glu607Gly missense_variant 11/12 -
NR_110451.1 n.1427A>G - non_coding_transcript_exon_variant 9/10 -