Variant #0001007032 (NC_000009.11:g.135171336T>C, NM_015046.5:c.6029A>G (SETX))

Chromosome 9
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.135171336T>C
DNA change (hg38) -
Published as -
ISCN -
DB-ID SETX_000060 See all 3 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs759806045
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 1.0E-5 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2024-08-28 17:28:02 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SETX NM_015046.5 +/. - c.6029A>G r.(?) p.(Asn2010Ser)


Screenscraping/webscraping (interacting with LOVD using scripts to download data) is strictly prohibited.
Use our APIs to retrieve data.