Variant #0000528583 (NC_000006.11:g.32811675G>A, NM_000593.5:c.*1681C>T (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.32811675G>A
DNA change (hg38) g.32843898G>A
Published as PSMB8(NM_148919.4):c.99C>T (p.Y33=)
ISCN -
DB-ID PSMB8_000022
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) Retrieve
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 2020-06-19 09:48:21 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TAP1 NM_000593.5 -?/. - c.*1681C>T r.(=) p.(=)
PSMB8 NM_148919.3 -?/. - c.99C>T r.(?) p.(Tyr33=)


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