Variant #0001791107 (NC_000019.9:g.49464363C>T, NC_000019.9(NM_138763.3):c.327+192C>T (BAX))

Chromosome 19
DNA change (genomic) (Relative to hg19 / GRCh37) g.49464363C>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID BAX_000052
Frequency 293/12770
Freq. EA 271/8476
Freq. AA 22/4294
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 16:45:39 +02:00 (CEST)
Date last edited 2013-05-06 02:14:04 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
BAX NM_138763.3 ?/? c.327+192C>T r.(=) p.(=)