Variant #0000860047 (NC_000005.9:g.96098026C>T, NM_016442.3:c.*878G>A (ERAP1))

Chromosome 5
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.96098026C>T
DNA change (hg38) -
Published as CAST(NM_001750.6):c.1882C>T (p.Q628*)
ISCN -
DB-ID CAST_000010
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
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     
CAST NM_001042440.2 +/. - c.1759C>T r.(?) p.(Gln587*)
ERAP1 NM_016442.3 +/. - c.*878G>A r.(=) p.(=)


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