Variant #0000720868 (NC_000006.11:g.32810015G>A, NM_000593.5:c.*3341C>T (TAP1))

Chromosome 6
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.32810015G>A
DNA change (hg38) -
Published as PSMB8(NM_148919.4):c.433C>T (p.R145C)
ISCN -
DB-ID PSMB8_000038
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) 0.00023 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 N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TAP2 NM_000544.3 ?/. - c.-3590C>T r.(?) p.(=)
TAP1 NM_000593.5 ?/. - c.*3341C>T r.(=) p.(=)
PSMB8 NM_148919.3 ?/. - c.433C>T r.(?) p.(Arg145Cys)


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