Variant #0001936116 (NC_000022.10:g.43089517C>T, NM_017436.4:c.441G>A (A4GALT))

Chromosome 22
DNA change (genomic) (Relative to hg19 / GRCh37) g.43089517C>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID A4GALT_000034
Frequency 63/13004
Freq. EA 1/8600
Freq. AA 62/4404
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 10:58:14 +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.441G>A r.(=) p.(=)