Variant #0000528579 (NC_000006.11:g.32808753G>A, NM_000593.5:c.*4603C>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.32808753G>A
DNA change (hg38) g.32840976G>A
Published as PSMB8(NM_004159.5):c.802C>T (p.R268W)
ISCN -
DB-ID PSMB8_000020
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) 6.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TAP2 NM_000544.3 ?/. - c.-2328C>T r.(?) p.(=)
TAP1 NM_000593.5 ?/. - c.*4603C>T r.(=) p.(=)
PSMB8 NM_148919.3 ?/. - c.814C>T r.(?) p.(Arg272Trp)


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