RGD:11599059 Rat Genome Database

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Variant: RGD:11599059 -  Homo sapiens

RGD ID: 11599059
RS ID: rs151270374
ClinVar ID: CV323800
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: GRIN2B  
Reference Nucleotide: C
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 12 13,714,487
GRCh38 12 13,561,553
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NC_000012.12:g.13561553C>G
NC_000012.11:g.13714487C>G
NG_031854.2:g.425460G>C
NM_000834.3:c.*1230G>C
More... 		11/01/2022 3 prime utr variant benign|likely benign|uncertain significance none provided
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:GRIN2B
Accession:NM_000834
Location:3UTRS;EXON

Gene Symbol:GRIN2B
Accession:XM_005253351
Location:3UTRS;EXON

Gene Symbol:
Accession:
Location:3UTRS;EXON

Gene Symbol:GRIN2B
Accession:NM_001413992
Location:3UTRS;EXON

Gene Symbol:GRIN2B
Accession:NM_001413994
Location:INTRON

Gene Symbol:GRIN2B
Accession:NM_001413995
Location:INTRON

Gene Symbol:GRIN2B
Accession:NM_001413993
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000262331 CLINVAR
  RCV002275023 CLINVAR
dbSNP (RS) rs151270374 CLINVAR
MedGen C3661900 CLINVAR
  CN239282 CLINVAR
NCBI Gene GRIN2B CLINVAR
OMIM 138252 CLINVAR