Variant #0000798871 (NC_000001.10:g.160261672G>A, NM_004371.3:c.3195C>T (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.160261672G>A
DNA change (hg38) -
Published as COPA(NM_001098398.2):c.3222C>T (p.S1074=)
ISCN -
DB-ID COPA_000055
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) 2.0E-5 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 2021-09-17 14:40:49 +02:00 (CEST)
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.-6758C>T r.(?) p.(=)
COPA NM_004371.3 -?/. - c.3195C>T r.(?) p.(Ser1065=)
NCSTN NM_015331.2 -?/. - c.-51515G>A r.(?) p.(=)


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