Variant #0000461191 (NC_000022.10:g.51065803G>A, NM_000487.5:c.256C>T (ARSA))

Chromosome 22
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Affects function
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.51065803G>A
DNA change (hg38) g.50627375G>A
Published as -
ISCN -
DB-ID ARSA_000008 See all 14 reported entries
Variant remarks 6% residual activity
Reference Journal: Cesani et al. (2009)
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Martina Cesani
Database submission license No license selected
Created by Martina Cesani
Date created 2014-07-22 12:31:42 +02:00 (CEST)
Date last edited 2020-07-17 16:21:50 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Protein level     
ARSA NM_000487.5 +/+ 2 c.256C>T r.(?) p.Arg86Trp -


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