Variant #0000785875 (NC_000014.8:g.32031331G>A, NM_025152.2:c.166G>A (NUBPL))

Chromosome 14
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.32031331G>A
DNA change (hg38) -
Published as -
ISCN -
DB-ID NUBPL_000017 See all 9 reported entries
Variant remarks lentiviral cDNA expression in fibroblasts gives stable protein able to restore CI activity
Reference PubMed: Tucker 2012
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00013 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 2021-05-19 09:13:43 +02:00 (CEST)
Date last edited 2021-05-19 09:14:02 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NUBPL NM_025152.2 -/. - c.166G>A r.(?) p.Gly56Arg


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