Variant #0000523433 (NC_000004.11:g.170988468_170988469insT, NC_000004.11(NM_016228.3):c.962+9_962+10insA (AADAT))

Chromosome 4
DNA change (genomic) (Relative to hg19 / GRCh37) g.170988468_170988469insT
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID AADAT_000028
Frequency 80/12520
Freq. EA 1/8254
Freq. AA 79/4266
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 16:25:12 +02:00 (CEST)
Date last edited 2018-08-23 01:49:17 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
AADAT NM_016228.3 ?/? c.962+9_962+10insA r.(=) p.(=)