RGD:150452570 Rat Genome Database

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Variant: RGD:150452570 -  Homo sapiens

RGD ID: 150452570
RS ID: rs769391
ClinVar ID: CV1254981
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: GAD1  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 2 171,709,430
GRCh38 2 170,852,920
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NG_021477.1:g.41231A>G
NC_000002.12:g.170852920A>G
NC_000002.11:g.171709430A>G
NM_000817.3:c.1263+128A>G
 11/11/2018 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:GAD1
Accession:XM_011510922
Location:INTRON

Gene Symbol:GAD1
Accession:XM_047443875
Location:INTRON

Gene Symbol:GAD1
Accession:NM_000817
Location:INTRON

Gene Symbol:GAD1
Accession:XM_047443874
Location:INTRON

Gene Symbol:GAD1
Accession:XM_017003756
Location:INTRON

Gene Symbol:GAD1
Accession:XM_017003758
Location:INTRON

Gene Symbol:GAD1
Accession:NM_013445
Location:INTRON

Gene Symbol:GAD1
Accession:XM_024452783
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001668040 CLINVAR
dbSNP (RS) rs769391 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene GAD1 CLINVAR
OMIM 605363 CLINVAR