Variant #0000447036 (NC_000009.11:g.119461480G>A, NM_012210.3:c.1459G>A (TRIM32))

Chromosome 9
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.119461480G>A
DNA change (hg38) g.116699201G>A
Published as -
ISCN -
DB-ID TRIM32_000001 See all 15 reported entries
Variant remarks YTH cloning in pGBKT7/pGADT7, no homo-dimerisation, no UBE2N binding; GFP-TRIM32 normal localization COS7
Reference PubMed: Saccone 2007
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 1.0E-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 2008-07-18 17:05:06 +02:00 (CEST)
Date last edited 2020-07-14 21:57:48 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TRIM32 NM_012210.3 +/. 2 c.1459G>A r.(?) p.(Asp487Asn)


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