Variant #0000802242 (NC_000005.9:g.95759019A>G, NM_000439.4:c.541T>C (PCSK1))

Chromosome 5
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.95759019A>G
DNA change (hg38) -
Published as PCSK1(NM_000439.4):c.541T>C (p.Y181H), PCSK1(NM_000439.5):c.541T>C (p.Y181H)
ISCN -
DB-ID ELL2_000002 See all 2 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) 0.00011 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 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PCSK1 NM_000439.4 ?/. - c.541T>C r.(?) p.(Tyr181His)
ELL2 NM_012081.5 ?/. - c.-461594T>C r.(?) p.(=)


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