Variant #0001785276 (NC_000019.9:g.47278967C>T, NM_001145144.1:c.742G>A (SLC1A5))

Chromosome 19
DNA change (genomic) (Relative to hg19 / GRCh37) g.47278967C>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID SLC1A5_000010
Frequency 1/13006
Freq. EA 1/8600
Freq. AA 0/4406
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 16:45:39 +02:00 (CEST)
Date last edited 2013-05-06 01:57:54 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
SLC1A5 NM_001145144.1 ?/? c.742G>A r.(?) p.(Ala248Thr)