Variant #0001613498 (NC_000017.10:g.57158552G>A, NM_015294.3:c.398C>T (TRIM37))

Chromosome 17
DNA change (genomic) (Relative to hg19 / GRCh37) g.57158552G>A
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID TRIM37_000120
Frequency 90/13006
Freq. EA 79/8600
Freq. AA 11/4406
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 16:44:12 +02:00 (CEST)
Date last edited 2013-05-05 18:35:18 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
TRIM37 NM_015294.3 ?/? c.398C>T r.(?) p.(Ala133Val)