Variant #0001532353 (NC_000017.10:g.902850T>C, NC_000017.10(NM_013337.2):c.508+26T>C (TIMM22))

Chromosome 17
DNA change (genomic) (Relative to hg19 / GRCh37) g.902850T>C
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID TIMM22_000038
Frequency 520/13006
Freq. EA 331/8600
Freq. AA 189/4406
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 15:21:51 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
TIMM22 NM_013337.2 ?/? c.508+26T>C r.(=) p.(=)