Variant #0000200467 (NC_000002.11:g.242735_242736insAACAAC, NC_000002.11(NM_015677.2):c.291+4802_291+4803insGTTGTT (SH3YL1))

Chromosome 2
DNA change (genomic) (Relative to hg19 / GRCh37) g.242735_242736insAACAAC
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID SH3YL1_000057
Frequency 17/8842
Freq. EA 14/5978
Freq. AA 3/2864
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 16:22:05 +02:00 (CEST)
Date last edited 2014-05-04 14:45:26 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
SH3YL1 NM_015677.2 ?/? c.291+4802_291+4803insGTTGTT r.(=) p.(=)