RGD:405174865 Rat Genome Database

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Variant: RGD:405174865 -  Homo sapiens

RGD ID: 405174865
ClinVar ID: CV2922970
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: PSAT1  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 9 80,943,890
GRCh38 9 78,328,974
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_058179.4:c.1008-7A>G
NM_021154.5:c.870-7A>G
NG_012165.1:g.36832A>G
NC_000009.12:g.78328974A>G
More... 		10/10/2023 intron variant likely benign
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV003587993 CLINVAR
MedGen C4015019 CLINVAR
NCBI Gene PSAT1 CLINVAR
OMIM 610936 CLINVAR
  616038 CLINVAR