Variant #0000000476 (NC_000008.10:g.11405576G>A, NM_001715.2:c.211G>A (BLK))

Chromosome 8
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Effect unknown
DNA change (genomic) (Relative to hg19 / GRCh37) g.11405576G>A
Reference -
DB-ID BLK_000002
Frequency -
Average frequency (gnomAD v.2.1.1) 0.01157 View details
Owner Florian Bayersdorfer
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Florian Bayersdorfer
Date created 2024-05-03 09:01:31 +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     
BLK NM_001715.2 ?/? 4 c.211G>A r.(?) p.(Ala71Thr)