Variant #0000743436 (NC_000007.13:g.48237906G>C, NM_152701.3:c.236G>C (ABCA13))

Chromosome 7
DNA change (genomic) (Relative to hg19 / GRCh37) g.48237906G>C
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID ABCA13_000013
Frequency 5/11932
Freq. EA 0/8220
Freq. AA 5/3712
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 2021-08-01 05:43:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
ABCA13 NM_152701.3 ?/? c.236G>C r.(?) p.(Gly79Ala)