Variant #0000000314 (NC_000005.9:g.78264868_78264901del, ARSB(NM_000046.3):c.427_460del)

Individual ID 00000098
Chromosome 5
Allele Parent #2
Affects function (as reported) Affects function
Affects function (by curator) Affects function
DNA change (genomic) (Relative to hg19 / GRCh37) g.78264868_78264901del
Reference -
DB-ID ARSB_000015
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
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Clinical classification     
ARSB NM_000046.3 +/+ - c.427_460del r.(?) p.(Val143Asnfs*30) pathogenic



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000101 DNA SEQ-NG ARSB 2 Variome.ir