Variant ID: 1-55527194-GT-CG

NM_174936.3(PCSK9):c.1828_1829delinsCG;(p.Val610Arg)

This variant was identified in 1 publication




Publications:


PCSK9 Variants in Familial Hypercholesterolemia: A Comprehensive Synopsis.

Frontiers In Genetics
Q Guo, X Feng, Y Zhou
Publication Date: 2020

Variant appearance in text: PCSK9: V610R
PubMed Link: 33173529
Variant Present in the following documents:
  • Main text
View BVdb publication page



Alternative transcript annotations:

Transcript cDNA Protein Consequence Exon Intron
ENST00000302118.5 c.1828_1829delinsCG p.Val610Arg missense_variant 11/12 -
ENST00000490692.1 n.2374_2375delinsCG - non_coding_transcript_exon_variant 7/8 -
ENST00000543384.1 c.*375_*376delinsCG - 3_prime_UTR_variant 9/10 -
NM_174936.4 c.1828_1829delinsCG p.Val610Arg missense_variant 11/12 -
NR_110451.1 n.1435_1436delinsCG - non_coding_transcript_exon_variant 9/10 -