Variant #0000507984 (NC_000001.10:g.55529215C>A, NM_174936.3:c.2037C>A (PCSK9))

Chromosome 1
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.55529215C>A
DNA change (hg38) g.55063542C>A
Published as PCSK9(NM_174936.4):c.2037C>A (p.C679*)
ISCN -
DB-ID PCSK9_000337
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00057 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-11-27 17:27:23 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
USP24 NM_015306.2 +/. - c.*5503G>T r.(=) p.(=)
PCSK9 NM_174936.3 +/. - c.2037C>A r.(?) p.(Cys679Ter)


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