Variant #0001014153 (NC_000005.9:g.96139428G>A, NM_016442.3:c.202C>T (ERAP1))

Chromosome 5
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.96139428G>A
DNA change (hg38) -
Published as ERAP1(NM_016442.5):c.202C>T (p.H68Y)
ISCN -
DB-ID CAST_000014
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) 8.0E-5 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 2024-10-29 21:08:56 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CAST NM_001042440.2 ?/. - c.*31108G>A r.(=) p.(=)
ERAP1 NM_016442.3 ?/. - c.202C>T r.(?) p.(His68Tyr)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.