RGD:407427999 Rat Genome Database

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Variant: RGD:407427999 -  Homo sapiens

RGD ID: 407427999
ClinVar ID: CV2848528
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: RCC1  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 1 28,858,701
GRCh38 1 28,532,189
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001048199.3:c.280A>G
NM_001269.6:c.280A>G
NM_001381865.2:c.280A>G
NM_001381866.2:c.280A>G
More...
01/11/2024 missense variant likely pathogenic

Variant Details
Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV004593302 CLINVAR
NCBI Gene RCC1 CLINVAR
OMIM 179710 CLINVAR