Variant #0000806605 (NC_000015.9:g.25616093A>G, NM_000462.3:c.1237T>C (UBE3A))

Chromosome 15
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.25616093A>G
DNA change (hg38) -
Published as UBE3A(NM_130838.1):c.1168T>C (p.L390=)
ISCN -
DB-ID UBE3A_001111
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) 2.0E-5 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
UBE3A NM_000462.3 -?/. - c.1237T>C r.(?) p.(Leu413=)
UBE3A NM_130839.2 -?/. - c.1228T>C r.(?) p.(Leu410=)


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