RGD:150459078 Rat Genome Database

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Variant: RGD:150459078 -  Homo sapiens

RGD ID: 150459078
RS ID: rs61143519
ClinVar ID: CV1248610
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: PSAT1  
Reference Nucleotide: T
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 9 80,923,629
GRCh38 9 78,308,713
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NG_012165.1:g.16571T>G
NC_000009.12:g.78308713T>G
NC_000009.11:g.80923629T>G
NM_058179.4:c.740+130T>G
More... 		11/12/2018 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:PSAT1
Accession:NM_058179
Location:INTRON

Gene Symbol:PSAT1
Accession:NM_021154
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001669220 CLINVAR
dbSNP (RS) rs61143519 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene PSAT1 CLINVAR
OMIM 610936 CLINVAR