Variant #0001014899 (NC_000012.11:g.109924382T>G, NC_000012.11(NM_183415.2):c.447+2T>G (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.109924382T>G
DNA change (hg38) -
Published as UBE3B(NM_130466.4):c.447+2T>G
ISCN -
DB-ID UBE3B_000051
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_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2024-10-29 21:08:56 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
UBE3B NM_130466.3 ?/. - c.447+2T>G r.spl? p.?
UBE3B NM_183415.2 ?/. - c.447+2T>G r.spl? p.?


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