Variant #0000553727 (NC_000015.9:g.25615917T>C, NM_000462.3:c.1413A>G (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.25615917T>C
DNA change (hg38) g.25370770T>C
Published as UBE3A(NM_000462.5):c.1413A>G (p.T471=)
ISCN -
DB-ID UBE3A_001084
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) 0.00127 View details
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 2024-04-19 20:27:30 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
UBE3A NM_000462.3 -/. - c.1413A>G r.(?) p.(Thr471=)
UBE3A NM_130839.2 -/. - c.1404A>G r.(?) p.(Thr468=)


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