Variant #0000282580 (NC_000003.11:g.139074528G>A, NM_004766.2:c.*2177C>T (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.139074528G>A
DNA change (hg38) g.139355686G>A
Published as MRPS22(NM_020191.4):c.883G>A (p.D295N)
ISCN -
DB-ID COPB2_000004
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) 0.0001 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
COPB2 NM_004766.2 -?/. - c.*2177C>T r.(=) p.(=)
MRPS22 NM_020191.2 -?/. - c.883G>A r.(?) p.(Asp295Asn)


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