Variant #0000091274 (NC_000022.10:g.51064630C>T, NM_000487.5:c.931G>A (ARSA))

Chromosome 22
Allele Both (homozygous)
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.51064630C>T
DNA change (hg38) g.50626202C>T
Published as 1574G>A G309S
ISCN -
DB-ID ARSA_000144 See all 9 reported entries
Variant remarks BHK cell cDNA expression cloning, normal targtting lysosomes, unstable, activity reduced to 0.13
Reference PubMed: Kreysing 1993
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 3.0E-5 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 15:52:31 +01:00 (CET)
Date last edited 2020-07-17 16:20:24 +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 +/. 5 c.931G>A r.(?) p.Gly311Ser -


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