RGD:14745473 Rat Genome Database

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Variant: RGD:14745473 -  Homo sapiens

RGD ID: 14745473
RS ID: rs2491158
ClinVar ID: CV664933
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: OAT  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 10 126,089,703
GRCh38 10 124,401,134
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_000274.4:c.1015-150C>T
NM_001322965.2:c.1015-150C>T
NM_001322966.2:c.1015-150C>T
NM_001322967.2:c.1015-150C>T
More... 		06/19/2018 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:OAT
Accession:NM_001322974
Location:INTRON

Gene Symbol:OAT
Accession:NM_001322970
Location:INTRON

Gene Symbol:OAT
Accession:NM_001171814
Location:INTRON

Gene Symbol:OAT
Accession:NM_001322965
Location:INTRON

Gene Symbol:OAT
Accession:NM_001322969
Location:INTRON

Gene Symbol:OAT
Accession:NM_001322971
Location:INTRON

Gene Symbol:OAT
Accession:NM_001322968
Location:INTRON

Gene Symbol:OAT
Accession:NM_000274
Location:INTRON

Gene Symbol:OAT
Accession:NM_001322966
Location:INTRON

Gene Symbol:OAT
Accession:NM_001322967
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000843409 CLINVAR
dbSNP (RS) rs2491158 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene OAT CLINVAR
OMIM 613349 CLINVAR