Variant #0000000379 (NC_000006.11:g.32808728C>T, NM_148919.3:c.*8G>A (PSMB8))

Chromosome 6
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Effect unknown
DNA change (genomic) (Relative to hg19 / GRCh37) g.32808728C>T
Reference -
DB-ID PSMB8_000002
Frequency -
Average frequency (gnomAD v.2.1.1) 0.00109 View details
Owner Florian Bayersdorfer
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Florian Bayersdorfer
Date created 2023-07-18 10:05:29 +00:00 (UTC)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PSMB8 NM_148919.3 ?/? - c.*8G>A r.(=) p.(=)