Variant #0001613448 (NC_000017.10:g.57126736A>G, NM_015294.3:c.1333T>C (TRIM37))

Chromosome 17
DNA change (genomic) (Relative to hg19 / GRCh37) g.57126736A>G
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID TRIM37_000070
Frequency 1/13006
Freq. EA 0/8600
Freq. AA 1/4406
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 18:35:10 +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.1333T>C r.(?) p.(Ser445Pro)