Variant #0001001254 (NC_000015.9:g.25601086G>C, NM_000462.3:c.2086C>G (UBE3A))

Chromosome 15
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.25601086G>C
DNA change (hg38) -
Published as UBE3A(NM_001354543.2):c.2017C>G (p.L673V)
ISCN -
DB-ID UBE3A_001127
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_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
UBE3A NM_000462.3 +?/. - c.2086C>G r.(?) p.(Leu696Val)
UBE3A NM_130839.2 +?/. - c.2077C>G r.(?) p.(Leu693Val)


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