Variant #0000503958 (NC_000001.10:g.160267162C>T, NM_004371.3:c.2234G>A (COPA))

Chromosome 1
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.160267162C>T
DNA change (hg38) g.160297372C>T
Published as COPA(NM_001098398.2):c.2261G>A (p.R754H)
ISCN -
DB-ID COPA_000017
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) 0.0003 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
COPA NM_004371.3 ?/. - c.2234G>A r.(?) p.(Arg745His)
NCSTN NM_015331.2 ?/. - c.-46025C>T r.(?) p.(=)


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