Variant #0000948044 (NC_000003.11:g.139108480C>T, NM_004766.2:c.-88G>A (COPB2))

Chromosome 3
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.139108480C>T
DNA change (hg38) -
Published as COPB2(NM_004766.2):c.-88G>A (p.(=))
ISCN -
DB-ID COPB2_000012
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) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2023-11-27 17:35:39 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RBP1 NM_002899.3 -?/. - c.*127989G>A r.(=) p.(=)
RBP2 NM_004164.2 -?/. - c.*63478G>A r.(=) p.(=)
COPB2 NM_004766.2 -?/. - c.-88G>A r.(?) p.(=)
NMNAT3 NM_178177.3 -?/. - c.*171372G>A r.(=) p.(=)


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