Variant #0008379184 (NC_000012.11:g.125612839G>A, NM_023928.3:c.1423+19delGinsA (AACS))

Chromosome 12
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.125612839G>A
DB-ID -
dbSNP ID rs900411
gnomAD frequency 78462/240084
gnomAD homozygote count 13532/55110
Average frequency (gnomAD v.2.1.1) Retrieve
Database submission license No license selected
Created by LOVD
Date created 2017-02-27 00:00:00 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
AACS NM_023928.3 ./. c.1423+19delGinsA r.(=) p.(=)