Variant #0000461205 (NC_000022.10:g.51064678C>T, NM_000487.5:c.883G>A (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.51064678C>T
DNA change (hg38) g.50626250C>T
Published as -
ISCN -
DB-ID ARSA_000024 See all 5 reported entries
Variant remarks 0% residual activity
Reference PubMed: Berna 2004, Journal: Berna 2004, ExPASy_054194
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 1.0E-5 View details
Owner Martina Cesani
Database submission license No license selected
Created by Martina Cesani
Date created 2014-07-31 18:02:06 +02:00 (CEST)
Date last edited 2020-07-17 16:20:32 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Protein level     
ARSA NM_000487.5 +/+ 5 c.883G>A r.(?) p.Gly295Ser -


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.