Variant #0001452120 (NC_000016.9:g.2378596C>T, NM_001089.2:c.-169G>A (ABCA3))

Chromosome 16
DNA change (genomic) (Relative to hg19 / GRCh37) g.2378596C>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID ABCA3_000440
Frequency 494/5732
Freq. EA 9/3980
Freq. AA 485/1752
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 09:37:51 +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.-169G>A r.(=) p.(=)