Variant #0001452048 (NC_000016.9:g.2369892A>G, NC_000016.9(NM_001089.2):c.614-51T>C (ABCA3))

Chromosome 16
DNA change (genomic) (Relative to hg19 / GRCh37) g.2369892A>G
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID ABCA3_000368
Frequency 2/12992
Freq. EA 0/8596
Freq. AA 2/4396
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 00:04:30 +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.614-51T>C r.(=) p.(=)