Variant #0000323068 (NC_000012.11:g.109924385_109924392del, NC_000012.11(NM_183415.2):c.447+5_447+12del (UBE3B))

Chromosome 12
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.109924385_109924392del
DNA change (hg38) g.109486580_109486587del
Published as UBE3B(NM_001270449.1):c.447+3_447+10del (p.?)
ISCN -
DB-ID UBE3B_000001
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-11-27 17:27:23 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
UBE3B NM_130466.3 ?/. - c.447+5_447+12del r.spl? p.?
UBE3B NM_183415.2 ?/. - c.447+5_447+12del r.spl? p.?


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