Variant #0001978229 (NC_000023.10:g.100615025G>T, NC_000023.10(NM_000061.2):c.839+51C>A (BTK))

Chromosome X
DNA change (genomic) (Relative to hg19 / GRCh37) g.100615025G>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID BTK_000044
Frequency 684/10563
Freq. EA 569/6728
Freq. AA 115/3835
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 10:11:56 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
BTK NM_000061.2 ?/? c.839+51C>A r.(=) p.(=)