Variant #0001978215 (NC_000023.10:g.100613694C>T, NC_000023.10(NM_000061.2):c.895-10G>A (BTK))

Chromosome X
DNA change (genomic) (Relative to hg19 / GRCh37) g.100613694C>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID BTK_000032
Frequency 3/10563
Freq. EA 3/6728
Freq. AA 0/3835
Average frequency (gnomAD v.2.1.1) -
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Ivo F.A.C. Fokkema
Date created 2013-05-03 16:50:35 +02:00 (CEST)
Date last edited 2013-05-06 10:11:55 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
BTK NM_000061.2 ?/? c.895-10G>A r.(=) p.(=)