Variant #0001068257 (NC_000003.11:g.181430218_181430237del, NM_003106.3:c.70_89del (SOX2))

Chromosome 3
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.181430218_181430237del
DNA change (hg38) -
Published as -
ISCN -
DB-ID SOX2_000006 See all 2 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs398123693
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2026-02-13 09:43:02 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SOX2 NM_003106.3 +/. - c.70_89del r.(?) p.(Asn24ArgfsTer65)


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