RGD:155965465 Rat Genome Database

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Variant: RGD:155965465 -  Homo sapiens

RGD ID: 155965465
ClinVar ID: CV2048789
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: PSAT1  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 9 80,943,115
GRCh38 9 78,328,199
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.1007+11C>T
NM_021154.5:c.870-782C>T
NG_012165.1:g.36057C>T
NC_000009.12:g.78328199C>T
More... 		06/22/2022 intron variant likely benign
Disease Annotations     Click to see Annotation Detail View


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

Gene Symbol:PSAT1
Accession:NM_021154
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV002776468 CLINVAR
MedGen C4015019 CLINVAR
NCBI Gene PSAT1 CLINVAR
OMIM 610936 CLINVAR
  616038 CLINVAR