Variant #0000604939 (NC_000001.10:g.160268981G>A, NM_004371.3:c.1741C>T (COPA))

Chromosome 1
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.160268981G>A
DNA change (hg38) g.160299191G>A
Published as COPA(NM_001098398.1):c.1768C>T (p.(Leu590=)), COPA(NM_001098398.2):c.1768C>T (p.L590=)
ISCN -
DB-ID COPA_000029 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) 0.0252 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-12-04 14:54:23 +01:00 (CET)
Date last edited 2022-05-09 15:51:19 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
COPA NM_004371.3 -/. - c.1741C>T r.(?) p.(Leu581=)
NCSTN NM_015331.2 -/. - c.-44206G>A r.(?) p.(=)


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