Variant #0000091277 (NC_000022.10:g.51065361C>A, NM_000487.5:c.585G>T (ARSA))

Chromosome 22
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.51065361C>A
DNA change (hg38) g.50626933C>A
Published as G>T (Trp193Cys)
ISCN -
DB-ID ARSA_000015 See all 15 reported entries
Variant remarks BHK cells expression cloning gives normal activity
Reference PubMed: Polten 1991, Journal: Polten 1991
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.05327 View details
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2016-03-25 16:56:41 +01:00 (CET)
Date last edited 2020-07-17 16:20:58 +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 -/. 3 c.585G>T r.(?) p.Trp195Cys -


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