Variant #0000461189 (NC_000022.10:g.51066047A>G, NM_000487.5:c.161T>C (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.51066047A>G
DNA change (hg38) g.50627619A>G
Published as -
ISCN -
DB-ID ARSA_000005
Variant remarks <1% residual activity
Reference PubMed: Cesani 2009, Journal: Cesani 2009, ExPASy_067414
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 11:52:21 +02:00 (CEST)
Date last edited 2020-07-17 16:21:58 +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 +/+ 1 c.161T>C r.(?) p.Leu54Pro -


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