Variant #0000743483 (NC_000007.13:g.48278822T>C, NC_000007.13(NM_152701.3):c.898-16T>C (ABCA13))

Chromosome 7
DNA change (genomic) (Relative to hg19 / GRCh37) g.48278822T>C
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID ABCA13_000060
Frequency 6/11948
Freq. EA 0/8208
Freq. AA 6/3740
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 16:28:58 +02:00 (CEST)
Date last edited 2018-08-23 12:45:32 +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.898-16T>C r.(=) p.(=)