Variant #0008378452 (NC_000012.11:g.125550238G>T, NM_023928.3:c.108G>T (AACS))

Chromosome 12
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.125550238G>T
DB-ID -
dbSNP ID rs763562803
gnomAD frequency 15/138702
gnomAD homozygote count 0/69334
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.108G>T r.(?) p.(Val36=)