RGD:597783372 Rat Genome Database

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Variant: RGD:597783372 -  Homo sapiens

RGD ID: 597783372
ClinVar ID: CV3686237
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: HTRA3  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 4 8,288,466
GRCh38 4 8,286,739
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_001297559.3:c.664A>G
NM_053044.5:c.664A>G
NC_000004.12:g.8286739A>G
NC_000004.11:g.8288466A>G
More... 		08/12/2024 missense variant uncertain significance AllHighlyPenetrant

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Database
Acc Id
Source(s)
ClinVar RCV004931402 CLINVAR
MedGen CN169374 CLINVAR
NCBI Gene HTRA3 CLINVAR
OMIM 608785 CLINVAR