Variant #0000580093 (NC_000017.10:g.66339822G>A, NM_014960.3:c.(296G>A) (ARSG))

Chromosome 17
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Effect unknown
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.66339822G>A
DNA change (hg38) g.68343681G>A
Published as -
ISCN -
DB-ID ARSG_000000 See all 3 reported entries
Variant remarks expression cloning HEK293T cells, sulfatase activity decreased by 0.75
Reference PubMed: Abitbol 2010
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency 91/181 cases
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 3.0E-5 View details
Owner Sara Mole
Database submission license No license selected
Created by Sara Mole
Date created 2012-11-02 17:42:00 +01:00 (CET)
Date last edited 2020-07-14 21:55:22 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ARSG NM_014960.3 +/? 3 c.(296G>A) r.(?) p.Arg99His


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