RGD:407529806 Rat Genome Database

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Variant: RGD:407529806 -  Homo sapiens

RGD ID: 407529806
ClinVar ID: CV3471602
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: ARAF  
Reference Nucleotide: G
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 X 47,422,704
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001256196.2:c.176G>T
NM_001256197.2:c.176G>T
NM_001654.5:c.176G>T
NG_016339.2:g.7189G>T
More... 		04/15/2024 missense variant uncertain significance AllHighlyPenetrant

Variant Details
Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV004656227 CLINVAR
MedGen CN169374 CLINVAR
NCBI Gene ARAF CLINVAR
OMIM 311010 CLINVAR