RGD:407507422 Rat Genome Database

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Variant: RGD:407507422 -  Homo sapiens

RGD ID: 407507422
ClinVar ID: CV3457673
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: MTO1  
Reference Nucleotide: C
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 6 74,176,240
GRCh38 6 73,466,517
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_001123226.2:c.446C>A
NM_012123.4:c.446C>A
NM_133645.3:c.446C>A
NG_032856.3:g.9782C>A
More... 		05/14/2024 missense variant uncertain significance
Object Symbol
Species
Term
Qualifier
Evidence
With
Reference
Notes
Source
Original Reference(s)
CV3457673Humangenetic disease  IAGP 8554872ClinVar Annotator: match by term: Inborn genetic diseasesClinVar 


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Database
Acc Id
Source(s)
ClinVar RCV004646808 CLINVAR
MedGen C0950123 CLINVAR
NCBI Gene MTO1 CLINVAR
OMIM 614667 CLINVAR