Variant #0000932977 (NC_000001.10:g.55509693G>A, NM_174936.3:c.385G>A (PCSK9))

Chromosome 1
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.55509693G>A
DNA change (hg38) -
Published as -
ISCN -
DB-ID PCSK9_000248 See all 2 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs778738291
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 2.0E-5 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2023-08-29 12:19:01 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PCSK9 NM_174936.3 ?/. - c.385G>A r.(?) p.(Asp129Asn)


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