Variant #0001936128 (NC_000022.10:g.43089742G>A, NM_017436.4:c.216C>T (A4GALT))

Chromosome 22
DNA change (genomic) (Relative to hg19 / GRCh37) g.43089742G>A
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID A4GALT_000046
Frequency 1/13000
Freq. EA 0/8596
Freq. AA 1/4404
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 16:50:05 +02:00 (CEST)
Date last edited 2018-08-23 12:18:10 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
A4GALT NM_017436.4 ?/? c.216C>T r.(=) p.(=)