Variant #0000999592 (NC_000012.11:g.109971274G>T, NM_183415.2:c.2926G>T (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.109971274G>T
DNA change (hg38) -
Published as UBE3B(NM_130466.3):c.2926G>T (p.(Val976Leu))
ISCN -
DB-ID UBE3B_000049
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 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
UBE3B NM_130466.3 ?/. - c.2926G>T r.(?) p.(Val976Leu)
UBE3B NM_183415.2 ?/. - c.2926G>T r.(?) p.(Val976Leu)


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