Variant #0001785269 (NC_000019.9:g.47278805del, NM_001145144.1:c.904del (SLC1A5))

Chromosome 19
DNA change (genomic) (Relative to hg19 / GRCh37) g.47278805del
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID SLC1A5_000003
Frequency 14/12518
Freq. EA 8/8254
Freq. AA 6/4264
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 16:45:39 +02:00 (CEST)
Date last edited 2013-05-06 01:57:54 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
SLC1A5 NM_001145144.1 ?/? c.904del r.(?) p.(Asp302Metfs*32)