Variant #0000000491 (NC_000005.9:g.78280791G>T, ARSB(NM_000046.3):c.281C>A)

Individual ID 00000264
Chromosome 5
Allele Both (homozygous)
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.78280791G>T
Reference -
DB-ID ARSB_000011 See all 4 reported entries
Average frequency (gnomAD v.2.1.1) Variant not found in online data sets
Owner Variome.ir
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Variome.ir
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Clinical classification     
ARSB NM_000046.3 ./. - c.281C>A r.(?) p.(Ser94*) pathogenic



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000267 DNA SEQ-NG ARSB 1 Variome.ir