Variant #0000455450 (NC_000001.10:g.26384973G>A, NM_032588.3:c.739C>T (TRIM63))

Chromosome 1
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.26384973G>A
DNA change (hg38) g.26058482G>A
Published as -
ISCN -
DB-ID TRIM63_000011 See all 11 reported entries
Variant remarks FLAG-tagged cDNA expression cloning and co-IP in HeLa cells showed near complete loss of autoubiquitination; other assays performed as well
Reference PubMed: Chen 2012
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00066 View details
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2019-02-09 22:28:23 +01:00 (CET)
Date last edited 2020-06-04 09:32:41 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TRIM63 NM_032588.3 +/. - c.739C>T r.(?) p.Gln247*


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