Variant #0001078482 (NC_000023.10:g.2876390C>T, NM_000047.2:c.110G>A (ARSE))

Chromosome X
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.2876390C>T
DNA change (hg38) -
Published as -
ISCN -
DB-ID ARSE_000123
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs148939283
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 3.0E-5 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2026-06-12 11:37:01 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ARSE NM_000047.2 -?/. - c.110G>A r.(?) p.(Arg37Gln)


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