Variant #0000254035 (NC_000005.9:g.95759173A>G, NC_000005.9(NM_000439.4):c.397-10T>C (PCSK1))

Chromosome 5
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.95759173A>G
DNA change (hg38) g.96423469A>G
Published as PCSK1(NM_000439.4):c.397-10T>C, PCSK1(NM_000439.5):c.397-10T>C
ISCN -
DB-ID PCSK1_000020 See all 3 reported entries
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) 0.00572 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PCSK1 NM_000439.4 -?/. - c.397-10T>C r.(=) p.(=)
ELL2 NM_012081.5 -?/. - c.-461748T>C r.(?) p.(=)


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