Variant #0000553732 (NC_000015.9:g.25616951_25616954del, NM_000462.3:c.381_384del (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.25616951_25616954del
DNA change (hg38) g.25371804_25371807del
Published as UBE3A(NM_130838.1):c.312_315delCTTA (p.Y104*)
ISCN -
DB-ID UBE3A_001088 See all 2 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) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +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.381_384del r.(?) p.(Tyr127Ter)
UBE3A NM_130839.2 +/. - c.372_375del r.(?) p.(Tyr124Ter)


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