Variant #0000163945 (NC_000021.8:g.34951753T>G, NM_017613.3:c.1466A>C (DONSON))

Chromosome 21
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.34951753T>G
DNA change (hg38) g.33579447T>G
Published as K489T
ISCN -
DB-ID DONSON_000003 See all 9 reported entries
Variant remarks expression cloning showed reduced protein levels, normal subcellular localization (0.9) and did not complement loss of endogenous DONSON by rescuing spontaneous fork stalling after DONSON depletion
Reference PubMed: Reynolds 2017, Journal: Reynolds 2017
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.001 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 2017-03-17 14:16:04 +01:00 (CET)
Date last edited 2020-07-16 22:09:02 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Haplotype     

RNA change     

Protein     
DONSON NM_017613.3 +/. 9 c.1466A>C - r.(?) p.Lys489Thr


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