Variant #0001613486 (NC_000017.10:g.57148360C>T, NC_000017.10(NM_015294.3):c.685-52G>A (TRIM37))

Chromosome 17
DNA change (genomic) (Relative to hg19 / GRCh37) g.57148360C>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID TRIM37_000108
Frequency 1/7270
Freq. EA 0/4618
Freq. AA 1/2652
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 18:35:17 +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.685-52G>A r.(=) p.(=)