Variant #0001070272 (NC_000003.11:g.11059621G>A, NM_003042.3:c.331G>A (SLC6A1))

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.11059621G>A
DNA change (hg38) -
Published as -
ISCN -
DB-ID SLC6A1_000079
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs1559622516
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 2026-03-10 11:34:01 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SLC6A1 NM_003042.3 +/. - c.331G>A r.(?) p.(Gly111Arg)


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