RGD:597712148 Rat Genome Database

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Variant: RGD:597712148 -  Homo sapiens

RGD ID: 597712148
ClinVar ID: CV3555224
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: MYT1  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 20 62,839,273
GRCh38 20 64,207,920
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_004535.3:c.724G>A
NC_000020.11:g.64207920G>A
NC_000020.10:g.62839273G>A
NM_004535.2:c.724G>A
More... 		11/27/2024 missense variant uncertain significance
Object Symbol
Species
Term
Qualifier
Evidence
With
Reference
Notes
Source
Original Reference(s)
CV3555224Humangenetic disease  IAGP 8554872ClinVar Annotator: match by term: Inborn genetic diseasesClinVar 


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Database
Acc Id
Source(s)
ClinVar RCV004959269 CLINVAR
MedGen C0950123 CLINVAR
NCBI Gene MYT1 CLINVAR
OMIM 600379 CLINVAR