Variant #0000921406 (NC_000009.11:g.107602813_107602814insT, NC_000009.11(NM_005502.3):c.814-14_814-13insA (ABCA1))

Chromosome 9
DNA change (genomic) (Relative to hg19 / GRCh37) g.107602813_107602814insT
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID ABCA1_000380
Frequency 1322/12516
Freq. EA 555/8254
Freq. AA 767/4262
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 16:29:58 +02:00 (CEST)
Date last edited 2018-08-23 07:34:19 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
ABCA1 NM_005502.3 ?/? c.814-14_814-13insA r.(=) p.(=)