Variant #0000000099 (NC_000008.10:g.11418928C>T, NM_001715.2:c.1147C>T (BLK))

Chromosome 8
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Affects function
DNA change (genomic) (Relative to hg19 / GRCh37) g.11418928C>T
Reference -
DB-ID BLK_000001
Frequency -
Average frequency (gnomAD v.2.1.1) 1.0E-5 View details
Owner Florian Bayersdorfer
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Florian Bayersdorfer
Date created 2020-03-03 14:40:48 +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 ?/+ 11 c.1147C>T r.(?) p.(Arg383*)