RGD:597702907 Rat Genome Database

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Variant: RGD:597702907 -  Homo sapiens

RGD ID: 597702907
ClinVar ID: CV3699151
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: LRAT  
Reference Nucleotide: C
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 4 155,665,489
GRCh38 4 154,744,337
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_001301645.2:c.11C>G
NM_004744.5:c.11C>G
NG_009110.1:g.5327C>G
NC_000004.12:g.154744337C>G
More... 		09/09/2024 missense variant uncertain significance
Object Symbol
Species
Term
Qualifier
Evidence
With
Reference
Notes
Source
Original Reference(s)
CV3699151Humangenetic disease  IAGP 8554872ClinVar Annotator: match by term: Inborn genetic diseasesClinVar 


.


Database
Acc Id
Source(s)
ClinVar RCV004988247 CLINVAR
MedGen C0950123 CLINVAR
NCBI Gene LRAT CLINVAR
OMIM 604863 CLINVAR