Variant #0000163948 (NC_000021.8:g.34955882G>C, NM_017613.3:c.876C>G (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.34955882G>C
DNA change (hg38) g.33583576G>C
Published as -
ISCN -
DB-ID DONSON_000007 See all 2 reported entries
Variant remarks expression cloning showed disrupted subcellular localization (0.1)
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 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 14:29:41 +01:00 (CET)
Date last edited 2020-07-16 22:09:09 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Haplotype     

RNA change     

Protein     
DONSON NM_017613.3 +/. 5 c.876C>G - r.(?) p.Phe292Leu


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.