Variant #0000301250 (NC_000006.11:g.32810792G>T, NM_000593.5:c.*2564C>A (TAP1))

Chromosome 6
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.32810792G>T
DNA change (hg38) g.32843015G>T
Published as PSMB8(NM_004159.5):c.210C>A (p.T70=)
ISCN -
DB-ID PSMB8_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) 0.00449 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 2018-01-15 20:58:59 +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     
TAP2 NM_000544.3 -?/. - c.-4367C>A r.(?) p.(=)
TAP1 NM_000593.5 -?/. - c.*2564C>A r.(=) p.(=)
PSMB8 NM_148919.3 -?/. - c.222C>A r.(?) p.(Thr74=)


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