Variant #0000478223 (NC_000005.9:g.69372372G>C, NM_017411.3:c.859G>C (SMN2))

Chromosome 5
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.69372372G>C
DNA change (hg38) g.70076545G>C
Published as -
ISCN -
DB-ID SMN2_000003 See all 6 reported entries
Variant remarks expression cloning mini-gene splicing construct shows significant increase exon 7 inclusion (from 0.50 to
0.70)
Reference PubMed: Prior 2009
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00325 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 2019-05-10 11:31:26 +02:00 (CEST)
Date last edited 2020-07-14 21:51:45 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SMN2 NM_017411.3 +/. - c.859G>C r.859g>c p.Gly287Arg


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