RGD:12841553 Rat Genome Database

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Variant: RGD:12841553 -  Homo sapiens

RGD ID: 12841553
RS ID: rs150851773
ClinVar ID: CV370803
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: GRIN1  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 9 140,033,910
GRCh38 9 137,139,458
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NG_011507.1:g.5302G>A
NC_000009.12:g.137139458G>A
NC_000009.11:g.140033910G>A
NM_000832.7:c.-29G>A
More... 		03/07/2016 5 prime utr variant likely benign AllHighlyPenetrant

Variant Details
Variant Transcripts
Gene Symbol:GRIN1
Accession:NM_001185090
Location:5UTRS;EXON

Gene Symbol:GRIN1
Accession:XM_005266072
Location:5UTRS;EXON

Gene Symbol:GRIN1
Accession:NM_001185091
Location:5UTRS;EXON

Gene Symbol:GRIN1
Accession:NM_021569
Location:5UTRS;EXON

Gene Symbol:GRIN1
Accession:NM_000832
Location:5UTRS;EXON

Gene Symbol:GRIN1
Accession:XM_005266071
Location:5UTRS;EXON

Gene Symbol:GRIN1
Accession:XM_005266073
Location:5UTRS;EXON

Gene Symbol:GRIN1
Accession:NM_007327
Location:5UTRS;EXON

Gene Symbol:GRIN1
Accession:XM_011518583
Location:5UTRS;EXON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000432787 CLINVAR
dbSNP (RS) rs150851773 CLINVAR
MedGen CN169374 CLINVAR
NCBI Gene GRIN1 CLINVAR
OMIM 138249 CLINVAR