Variant #0000354928 (NC_000005.9:g.81572002A>T, NM_001025.4:c.358T>A (RPS23))

Chromosome 5
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Probably does not affect function
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.81572002A>T
DNA change (hg38) g.82276183A>T
Published as -
ISCN -
DB-ID RPS23_000002 See all 3 reported entries
Variant remarks expression cloning in yeast (confirmed) and E. coli (confirmed) indicate the variant does not influence function
Reference -
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Marc Pieterse
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2018-02-22 14:24:05 +01:00 (CET)
Date last edited 2020-07-14 21:50:58 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RPS23 NM_001025.4 -?/-? 4 c.358T>A r.(?) p.Phe120Ile


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