Variant ID: 1-55505571-C-CCTG

NM_174936.3(PCSK9):c.61_62insCTG;(p.Leu21delinsProVal)

This variant was identified in 1 publication




Publications:


Differential effects of PCSK9 loss of function variants on serum lipid and PCSK9 levels in Caucasian and African Canadian populations.

Lipids In Health And Disease
J Mayne, TC Ooi, A Raymond, M Cousins, L Bernier, T Dewpura, F Sirois, M Mbikay, J Davignon, M Chr├ętien
Publication Date: 2013-05-10

Variant appearance in text: PCSK9: 61_63insCTG
PMID: 23663650
View BVdb publication page



Alternative transcript annotations:

Transcript cDNA Protein Consequence Exon Intron
ENST00000302118.5 c.61_62insCTG p.Leu21delinsProVal protein_altering_variant 1/12 -
ENST00000452118.2 c.61_62insCTG p.Leu21delinsProVal protein_altering_variant 1/6 -
NM_174936.4 c.61_62insCTG p.Leu21delinsProVal protein_altering_variant 1/12 -
- - TF_binding_site_variant - -