Variant #0001062625 (NC_000003.11:g.139078173T>G, NM_004766.2:c.2242A>C (COPB2))

Chromosome 3
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.139078173T>G
DNA change (hg38) -
Published as -
ISCN -
DB-ID COPB2_000026
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs1941366039
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2026-01-07 10:58:02 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
COPB2 NM_004766.2 ?/. - c.2242A>C r.(?) p.(Thr748Pro)


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