Variant #0000882870 (NC_000001.10:g.160264593C>T, NM_004371.3:c.2531G>A (COPA))

Chromosome 1
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.160264593C>T
DNA change (hg38) -
Published as COPA(NM_001098398.2):c.2558G>A (p.G853D), COPA(NM_004371.4):c.2531G>A (p.G844D)
ISCN -
DB-ID COPA_000015 See all 2 reported entries
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) 0.00063 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 2022-11-01 13:01:21 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PEX19 NM_002857.3 -?/. - c.-9679G>A r.(?) p.(=)
COPA NM_004371.3 -?/. - c.2531G>A r.(?) p.(Gly844Asp)
NCSTN NM_015331.2 -?/. - c.-48594C>T r.(?) p.(=)


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