Variant #0000319226 (NC_000015.9:g.25616729C>T, NM_000462.3:c.601G>A (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.25616729C>T
DNA change (hg38) g.25371582C>T
Published as UBE3A(NM_000462.3):c.601G>A (p.(Ala201Thr)), UBE3A(NM_000462.5):c.601G>A (p.A201T), UBE3A(NM_130838.1):c.532G>A (p.A178T)
ISCN -
DB-ID UBE3A_001005 See all 4 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) 0.0117 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 2018-01-15 20:58:59 +01:00 (CET)
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.601G>A r.(?) p.(Ala201Thr)
UBE3A NM_130839.2 -/. - c.592G>A r.(?) p.(Ala198Thr)


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