Variant #0000964125 (NC_000006.11:g.32810794T>A, NM_000593.5:c.*2562A>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.32810794T>A
DNA change (hg38) -
Published as PSMB8(NM_004159.4):c.208A>T (p.(Thr70Ser)), PSMB8(NM_004159.5):c.208A>T (p.T70S), PSMB8(NM_148919.4):c.220A>T (p.T74S)
ISCN -
DB-ID PSMB8_000010 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) 0.00449 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2024-02-26 20:06:56 +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.-4369A>T r.(?) p.(=)
TAP1 NM_000593.5 ?/. - c.*2562A>T r.(=) p.(=)
PSMB8 NM_148919.3 ?/. - c.220A>T r.(?) p.(Thr74Ser)


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