Variant #0001068947 (NC_000015.9:g.25615745G>A, NM_130839.2:c.1576C>T (UBE3A))

Chromosome 15
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.25615745G>A
DNA change (hg38) -
Published as -
ISCN -
DB-ID UBE3A_001100 See all 2 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs1064793307
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2026-03-04 16:47:01 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
UBE3A NM_130839.2 +/. - c.1576C>T r.(?) p.(Arg526Cys)


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