Variant #0000719221 (NC_000003.11:g.139071543C>T, NM_004766.2:c.*5162G>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.139071543C>T
DNA change (hg38) -
Published as MRPS22(NM_020191.3):c.787C>T (p.R263C)
ISCN -
DB-ID COPB2_000006
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) 0.00039 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-02-08 18:36:18 +01:00 (CET)
Date last edited 2021-09-29 09:25:33 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
COPB2 NM_004766.2 ?/. - c.*5162G>A r.(=) p.(=)
MRPS22 NM_020191.2 ?/. - c.787C>T r.(?) p.(Arg263Cys)


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