Variant #0001013821 (NC_000003.11:g.139077636C>T, NM_004766.2:c.2503G>A (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.139077636C>T
DNA change (hg38) -
Published as COPB2(NM_004766.3):c.2503G>A (p.V835I)
ISCN -
DB-ID COPB2_000017
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2024-10-29 20:49:11 +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.2503G>A r.(?) p.(Val835Ile)
MRPS22 NM_020191.2 ?/. - c.*1780C>T r.(=) p.(=)


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