RGD:150332343 Rat Genome Database

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Variant: RGD:150332343 -  Homo sapiens

RGD ID: 150332343
RS ID: rs2981359
ClinVar ID: CV1169086
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: SLC6A3  
Reference Nucleotide: G
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 5 1,442,732
GRCh38 5 1,442,617
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NC_000005.9:g.1442732G>C
NC_000005.10:g.1442617G>C
NG_015885.1:g.7812C>G
NM_001044.5:c.286+295C>G
 07/05/2018 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 RCV001536836 CLINVAR
dbSNP (RS) rs2981359 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene SLC6A3 CLINVAR
OMIM 126455 CLINVAR