Variant #0000720574 (NC_000005.9:g.96062567A>T, NM_016442.3:c.*36337T>A (ERAP1))

Chromosome 5
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.96062567A>T
DNA change (hg38) -
Published as CAST(NM_001042440.5):c.271-626A>T
ISCN -
DB-ID CAST_000009
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) 0.00022 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2021-02-08 18:36:18 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CAST NM_001042440.2 -?/. - c.271-626A>T r.(=) p.(=)
ERAP1 NM_016442.3 -?/. - c.*36337T>A r.(=) p.(=)


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