Variant #0000743472 (NC_000007.13:g.48273623T>G, NM_152701.3:c.772T>G (ABCA13))

Chromosome 7
DNA change (genomic) (Relative to hg19 / GRCh37) g.48273623T>G
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID ABCA13_000049
Frequency 1/11952
Freq. EA 1/8228
Freq. AA 0/3724
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 16:28:58 +02:00 (CEST)
Date last edited 2025-01-02 23:14:18 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
ABCA13 NM_152701.3 ?/? c.772T>G r.(?) p.(Tyr258Asp)