Variant #0000981120 (NC_000015.9:g.25616152T>C, NM_000462.3:c.1178A>G (UBE3A))

Chromosome 15
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.25616152T>C
DNA change (hg38) -
Published as UBE3A(NM_130839.5):c.1169A>G (p.(Asn390Ser))
ISCN -
DB-ID UBE3A_001125
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 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-04-19 20:27:30 +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.1178A>G r.(?) p.(Asn393Ser)
UBE3A NM_130839.2 ?/. - c.1169A>G r.(?) p.(Asn390Ser)


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