Variant #0000993176 (NC_000003.11:g.119361412T>C, NC_000003.11(NM_001369919.2):c.*44-4A>G (POPDC2))

Chromosome 3
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.119361412T>C
DNA change (hg38) g.119642565T>C
Published as POPDC2(NM_001369919.2):c.*44-4A>G
ISCN -
DB-ID POPDC2_000002
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) 0.04797 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 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited 2025-07-07 12:23:26 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
POPDC2 NM_001369919.2 -/. - c.*44-4A>G r.spl? p.?


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.