Variant #0000857103 (NC_000001.10:g.160263172T>C, NC_000001.10(NM_004371.3):c.2754+4A>G (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.160263172T>C
DNA change (hg38) -
Published as COPA(NM_004371.4):c.2754+4A>G
ISCN -
DB-ID COPA_000061
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) 0.00262 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 2022-05-09 15:51:19 +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.-8258A>G r.(?) p.(=)
COPA NM_004371.3 -?/. - c.2754+4A>G r.spl? p.?
NCSTN NM_015331.2 -?/. - c.-50015T>C r.(?) p.(=)


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