RGD:28905627 Rat Genome Database

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Variant: RGD:28905627 -  Homo sapiens

RGD ID: 28905627
RS ID: rs189106205
ClinVar ID: CV877126
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: SLC6A4  
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 17 28,522,771
GRCh38 17 30,195,753
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001045.6:c.*2703A>G
NG_011747.2:g.45184A>G
NC_000017.11:g.30195753T>C
NC_000017.10:g.28522771T>C
More... 		01/12/2018 3 prime utr variant likely benign behavioral disorder
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:SLC6A4
Accession:NM_001045
Location:3UTRS;EXON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001126624 CLINVAR
dbSNP (RS) rs189106205 CLINVAR
MedGen C0004930 CLINVAR
NCBI Gene SLC6A4 CLINVAR
OMIM 182138 CLINVAR