Variant #0000910824 (NC_000001.10:g.160249868dup, NM_004371.3:c.*10079dup (COPA))

Chromosome 1
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.160249868dup
DNA change (hg38) -
Published as PEX19(NM_002857.3):c.763dupA (p.M255Nfs*25), PEX19(NM_002857.4):c.763dupA (p.M255Nfs*25)
ISCN -
DB-ID PEX19_000001 See all 3 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) Retrieve
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2023-01-11 15:44:22 +01:00 (CET)
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.763dup r.(?) p.(Met255Asnfs*25)
COPA NM_004371.3 +/. - c.*10079dup r.(?) p.(=)


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