RGD:401772325 Rat Genome Database

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Variant: RGD:401772325 -  Homo sapiens

RGD ID: 401772325
ClinVar ID: CV2719606
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: CYP3A4  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 7 99,377,707
GRCh38 7 99,780,084
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_000776.1:c.73T>C
NM_001202855.3:c.73T>C
NM_017460.6:c.73T>C
NG_008421.1:g.9102T>C
More... 		06/05/2023 missense variant uncertain significance AllHighlyPenetrant

Variant Details
Variant Transcripts
Gene Symbol:CYP3A4
Accession:NM_001202855
Location:EXON

Gene Symbol:CYP3A4
Accession:NM_017460
Location:EXON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV004327275 CLINVAR
MedGen CN169374 CLINVAR
NCBI Gene CYP3A4 CLINVAR
OMIM 124010 CLINVAR