Variant #0000546381 (NC_000012.11:g.109958961C>T, NM_183415.2:c.2085C>T (UBE3B))

Chromosome 12
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.109958961C>T
DNA change (hg38) g.109521156C>T
Published as UBE3B(NM_130466.3):c.2085C>T (p.Y695=)
ISCN -
DB-ID UBE3B_000028
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) 0.00049 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 2019-07-18 18:22:55 +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.2085C>T r.(?) p.(Tyr695=)
UBE3B NM_183415.2 -?/. - c.2085C>T r.(?) p.(Tyr695=)


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