Variant ID: 1-55518329-AA-GC

NM_174936.3(PCSK9):c.664_665delinsGC;(p.Lys222Ala)

This variant was identified in 1 publication




Publications:


Investigations on the evolutionary conservation of PCSK9 reveal a functionally important protrusion.

The Febs Journal
J Cameron, ├śL Holla, KE Berge, MA Kulseth, T Ranheim, TP Leren, JK Laerdahl
Publication Date: 2008-08

Variant appearance in text: PCSK9: K222A
PubMed Link: 18631360
Variant Present in the following documents:
  • Supplemental file
  • Main text
View BVdb publication page



Alternative transcript annotations:

Transcript cDNA Protein Consequence Exon Intron
ENST00000302118.5 c.664_665delinsGC p.Lys222Ala missense_variant 5/12 -
ENST00000452118.2 c.*308_*309delinsGC - 3_prime_UTR_variant 6/6 -
ENST00000490692.1 n.1485_1486delinsGC - non_coding_transcript_exon_variant 2/8 -
ENST00000543384.1 c.64_65delinsGC p.Lys22Ala missense_variant 3/10 -
NM_174936.4 c.664_665delinsGC p.Lys222Ala missense_variant 5/12 -
NR_110451.1 n.323_324delinsGC - non_coding_transcript_exon_variant 3/10 -