Variant #0000455452 (NC_000001.10:g.26387768G>C, NM_032588.3:c.390C>G (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.26387768G>C
DNA change (hg38) g.26061277G>C
Published as -
ISCN -
DB-ID TRIM63_000012 See all 3 reported entries
Variant remarks FLAG-tagged cDNA expression cloning and co-IP in HeLa cells showed 0.70 reduced 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) 5.0E-5 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 22:23:09 +01:00 (CET)
Date last edited 2020-06-04 09:32:53 +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.390C>G r.(?) p.Ile130Met


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