Variant #0001078358 (NC_000009.11:g.131356486G>A, NM_001130438.2:c.3248G>A (SPTAN1))

Chromosome 9
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.131356486G>A
DNA change (hg38) -
Published as -
ISCN -
DB-ID WDR34_000136 See all 2 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs369611161
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 2.0E-5 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2026-06-03 15:12:01 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SPTAN1 NM_001130438.2 ?/. - c.3248G>A r.(?) p.(Arg1083His)


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