Variant #0000248289 (NC_000022.10:g.51065404A>C, NM_000487.5:c.542T>G (ARSA))

Chromosome 22
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.51065404A>C
DNA change (hg38) g.50626976A>C
Published as ARSA(NM_000487.5):c.542T>G (p.(Ile181Ser)), ARSA(NM_000487.6):c.542T>G (p.I181S)
ISCN -
DB-ID ARSA_000115 See all 49 reported entries
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00023 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2025-02-07 18:57:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Protein level     
ARSA NM_000487.5 +/. - c.542T>G r.(?) p.(Ile181Ser) -


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