RGD:8646132 Rat Genome Database

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Variant: RGD:8646132 -  Homo sapiens

RGD ID: 8646132
RS ID: rs62638206
ClinVar ID: CV105545
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: GRM6  
Reference Nucleotide: C
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 5 178,418,785
GRCh38 5 178,991,784
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NG_008105.1:g.8340G>T
NC_000005.10:g.178991784C>A
NC_000005.9:g.178418785C>A
NM_000843.3:c.721+83G>T
More... 		intron|intron variant not provided none provided

Variant Details
Variant Transcripts
Gene Symbol:GRM6
Accession:NM_000843
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000086061 CLINVAR
dbSNP (RS) rs62638206 CLINVAR
MedGen CN517202 CLINVAR
NCBI Gene GRM6 CLINVAR
OMIM 604096 CLINVAR