Variant #0001613467 (NC_000017.10:g.57138449T>A, NM_015294.3:c.963A>T (TRIM37))

Chromosome 17
DNA change (genomic) (Relative to hg19 / GRCh37) g.57138449T>A
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID TRIM37_000089
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 18:35:12 +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.963A>T r.(=) p.(=)