RGD:150494313 Rat Genome Database

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Variant: RGD:150494313 -  Homo sapiens

RGD ID: 150494313
RS ID: rs41277899
ClinVar ID: CV1267329
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: PSAT1  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 9 80,921,145
GRCh38 9 78,306,229
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_021154.5:c.398-85C>T
NM_058179.4:c.398-85C>T
NG_012165.1:g.14087C>T
NC_000009.12:g.78306229C>T
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 RCV001688357 CLINVAR
dbSNP (RS) rs41277899 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene PSAT1 CLINVAR
OMIM 610936 CLINVAR