Variant ID: 1-55505547-CT-GC

NM_174936.3(PCSK9):c.37_38delinsGC;(p.Leu13Ala)

This variant was identified in 1 publication




Publications:


Atherosclerosis.

Arteriosclerosis, Thrombosis, And Vascular Biology
H Lu, A Daugherty
Publication Date: 2015-03

Variant appearance in text: PCSK9: L13a
PMID: 25717174
View BVdb publication page



Alternative transcript annotations:

Transcript cDNA Protein Consequence Exon Intron
ENST00000302118.5 c.37_38delinsGC p.Leu13Ala missense_variant 1/12 -
ENST00000452118.2 c.37_38delinsGC p.Leu13Ala missense_variant 1/6 -
NM_174936.4 c.37_38delinsGC p.Leu13Ala missense_variant 1/12 -
- - TF_binding_site_variant - -