Variant #0000339767 (NC_000015.9:g.25602030G>A, NM_000462.3:c.1776C>T (UBE3A))

Chromosome 15
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.25602030G>A
DNA change (hg38) g.25356883G>A
Published as UBE3A(NM_000462.5):c.1776C>T (p.Y592=), UBE3A(NM_001354543.1):c.1707C>T (p.Y569=), UBE3A(NM_130838.1):c.1707C>T (p.Y569=)
ISCN -
DB-ID UBE3A_001039 See all 3 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) 0.00076 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2024-04-19 20:27:30 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
UBE3A NM_000462.3 -/. - c.1776C>T r.(?) p.(Tyr592=)
UBE3A NM_130839.2 -/. - c.1767C>T r.(?) p.(Tyr589=)


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