Variant #0000805510 (NC_000012.11:g.109949046_109949047del, NM_183415.2:c.1894_1895del (UBE3B))

Chromosome 12
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.109949046_109949047del
DNA change (hg38) -
Published as UBE3B(NM_130466.3):c.1894_1895delAG (p.R632Gfs*67)
ISCN -
DB-ID UBE3B_000039
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) 1.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-09-17 14:40:49 +02:00 (CEST)
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.1894_1895del r.(?) p.(Arg632Glyfs*67)
UBE3B NM_183415.2 +?/. - c.1894_1895del r.(?) p.(Arg632Glyfs*67)


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