Variant #0000425138 (NC_000003.11:g.137849640T>C, NC_000003.11(NM_016161.2):c.408+51A>G (A4GNT))

Chromosome 3
DNA change (genomic) (Relative to hg19 / GRCh37) g.137849640T>C
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID A4GNT_000029
Frequency 2/12926
Freq. EA 2/8536
Freq. AA 0/4390
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 16:23:53 +02:00 (CEST)
Date last edited 2018-08-23 12:54:44 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
A4GNT NM_016161.2 ?/? c.408+51A>G r.(=) p.(=)