Variant #0000673986 (NC_000006.11:g.83074790G>A, NM_001166392.1:c.112G>A (TPBG))

Chromosome 6
DNA change (genomic) (Relative to hg19 / GRCh37) g.83074790G>A
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID TPBG_000003
Frequency 1/12774
Freq. EA 0/8462
Freq. AA 1/4312
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 16:27:59 +02:00 (CEST)
Date last edited 2013-05-04 10:07:26 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
TPBG NM_001166392.1 ?/? c.112G>A r.(?) p.(Ala38Thr)