Variant ID: 1-55512253-AGC-CAA

NM_174936.3(PCSK9):c.457_459delinsCAA;(p.Ser153Gln)

This variant was identified in 1 publication




Publications:


Stepwise processing analyses of the single-turnover PCSK9 protease reveal its substrate sequence specificity and link clinical genotype to lipid phenotype.

The Journal Of Biological Chemistry
JS Chorba, AM Galvan, KM Shokat
Publication Date: 2018-02-09

Variant appearance in text: PCSK9: S153Q
PMID: 29259136
View BVdb publication page



Alternative transcript annotations:

Transcript cDNA Protein Consequence Exon Intron
ENST00000302118.5 c.457_459delinsCAA p.Ser153Gln missense_variant 3/12 -
ENST00000452118.2 c.457_459delinsCAA p.Ser153Gln missense_variant 3/6 -
ENST00000543384.1 c.-77-5698_-77-5696delinsCAA - intron_variant - 1/9
NM_174936.4 c.457_459delinsCAA p.Ser153Gln missense_variant 3/12 -
NR_110451.1 n.183-5698_183-5696delinsCAA - intron_variant,non_coding_transcript_variant - 1/9