RGD:150333238 Rat Genome Database

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Variant: RGD:150333238 -  Homo sapiens

RGD ID: 150333238
RS ID: rs8179029
ClinVar ID: CV1169080
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: SLC6A3  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 5 1,409,985
GRCh38 5 1,409,870
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NG_015885.1:g.40559G>A
NC_000005.10:g.1409870C>T
NC_000005.9:g.1409985C>T
NM_001044.5:c.1270-21G>A
 08/14/2018 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:SLC6A3
Accession:NM_001044
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001537227 CLINVAR
dbSNP (RS) rs8179029 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene SLC6A3 CLINVAR
OMIM 126455 CLINVAR