Variant ID: 1-55527190-C-T

NM_174936.3(PCSK9):c.1824C>T;(p.Cys608Cys)

This variant was identified in 1 publication



Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP

Publications:

Alternative transcript annotations:

Transcript cDNA Protein Consequence Exon Intron
ENST00000302118.5 c.1824C>T p.Cys608= synonymous_variant 11/12 -
ENST00000490692.1 n.2370C>T - non_coding_transcript_exon_variant 7/8 -
ENST00000543384.1 c.*371C>T - 3_prime_UTR_variant 9/10 -
NM_174936.4 c.1824C>T p.Cys608= synonymous_variant 11/12 -
NR_110451.1 n.1431C>T - non_coding_transcript_exon_variant 9/10 -