Variant #0001685399 (NC_000019.9:g.1044753T>C, NC_000019.9(NM_019112.3):c.1215+10T>C (ABCA7))

Chromosome 19
DNA change (genomic) (Relative to hg19 / GRCh37) g.1044753T>C
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID ABCA7_000100
Frequency 9046/12948
Freq. EA 5904/8576
Freq. AA 3142/4372
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 16:45:39 +02:00 (CEST)
Date last edited 2018-08-23 05:17:16 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
ABCA7 NM_019112.3 ?/? c.1215+10T>C r.(=) p.(=)