Variant #0000604938 (NC_000001.10:g.160265582T>G, NM_004371.3:c.2420A>C (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.160265582T>G
DNA change (hg38) g.160295792T>G
Published as COPA(NM_001098398.2):c.2447A>C (p.N816T), COPA(NM_004371.4):c.2420A>C (p.N807T)
ISCN -
DB-ID COPA_000028 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) 0.00051 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 2019-12-04 14:54:23 +01:00 (CET)
Date last edited 2023-04-16 21:50:28 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PEX19 NM_002857.3 -?/. - c.-10668A>C r.(?) p.(=)
COPA NM_004371.3 -?/. - c.2420A>C r.(?) p.(Asn807Thr)
NCSTN NM_015331.2 -?/. - c.-47605T>G r.(?) p.(=)


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