Variant #0000802535 (NC_000006.11:g.32810485_32810486del, NM_000593.5:c.*2871_*2872del (TAP1))

Chromosome 6
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.32810485_32810486del
DNA change (hg38) -
Published as PSMB8(NM_004159.5):c.359_360delGT (p.C120Sfs*54)
ISCN -
DB-ID PSMB8_000040
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 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TAP2 NM_000544.3 +?/. - c.-4060_-4059del r.(?) p.(=)
TAP1 NM_000593.5 +?/. - c.*2871_*2872del r.(=) p.(=)
PSMB8 NM_148919.3 +?/. - c.371_372del r.(?) p.(Cys124Serfs*54)


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