Variant #0000200437 (NC_000002.11:g.230990G>T, NC_000002.11(NM_015677.2):c.702+33C>A (SH3YL1))

Chromosome 2
DNA change (genomic) (Relative to hg19 / GRCh37) g.230990G>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID SH3YL1_000026
Frequency 3/11940
Freq. EA 0/8200
Freq. AA 3/3740
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 2014-02-03 06:27:05 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
SH3YL1 NM_015677.2 ?/? c.702+33C>A r.(=) p.(=)