Variant #0000299925 (NC_000001.10:g.160318835G>A, NM_004371.3:c.-5875C>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.160318835G>A
DNA change (hg38) g.160349045G>A
Published as NCSTN(NM_015331.3):c.237G>A (p.E79=)
ISCN -
DB-ID NCSTN_000005
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) 0.00695 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +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.-5875C>T r.(?) p.(=)
NCSTN NM_015331.2 -?/. - c.237G>A r.(?) p.(Glu79=)


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