Variant #0001014152 (NC_000005.9:g.95730555G>C, NC_000005.9(NM_000439.4):c.1884+13C>G (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.95730555G>C
DNA change (hg38) -
Published as PCSK1(NM_000439.5):c.1884+13C>G
ISCN -
DB-ID ELL2_000039
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) 3.0E-5 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 2024-10-29 21:08:56 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PCSK1 NM_000439.4 -?/. - c.1884+13C>G r.(=) p.(=)
ELL2 NM_012081.5 -?/. - c.-433130C>G r.(?) p.(=)


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