RGD:11656462 Rat Genome Database

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Variant: RGD:11656462 -  Homo sapiens

RGD ID: 11656462
RS ID: rs886060542
ClinVar ID: CV303577
Genic Status: INTERGENIC
Type: SNV (SO:0001483) 
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 5 36,606,653
GRCh38 5 36,606,551
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NG_015890.1:g.5197C>T
NC_000005.10:g.36606551C>T
NC_000005.9:g.36606653C>T
NM_001166695.2:c.-280C>T
More... 		06/14/2016 5 prime utr variant uncertain significance EA syndrome; Episodic Ataxia syndrome
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000333348 CLINVAR
dbSNP (RS) rs886060542 CLINVAR
MedGen C1720189 CLINVAR
NCBI Gene SLC1A3 CLINVAR
OMIM 600111 CLINVAR