Variant #0000200432 (NC_000002.11:g.229986T>C, NM_015677.2:c.761A>G (SH3YL1))

Chromosome 2
DNA change (genomic) (Relative to hg19 / GRCh37) g.229986T>C
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID SH3YL1_000022
Frequency 17/11946
Freq. EA 17/8214
Freq. AA 0/3732
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 2014-05-03 19:45:41 +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.761A>G r.(?) p.(Gln254Arg)