Variant #0001452060 (NC_000016.9:g.2373700_2373701del, NC_000016.9(NM_001089.2):c.448-12_448-11del (ABCA3))

Chromosome 16
DNA change (genomic) (Relative to hg19 / GRCh37) g.2373700_2373701del
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID ABCA3_000380
Frequency 1/12518
Freq. EA 1/8254
Freq. AA 0/4264
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 16:42:42 +02:00 (CEST)
Date last edited 2018-08-23 01:44:37 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
ABCA3 NM_001089.2 ?/? c.448-12_448-11del r.(=) p.(=)