RGD:150495740 Rat Genome Database

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Variant: RGD:150495740 -  Homo sapiens

RGD ID: 150495740
RS ID: rs4820079
ClinVar ID: CV1272707
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: FBXO7  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 22 32,879,617
GRCh38 22 32,483,630
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001033024.2:c.181-267G>T
NM_012179.4:c.418-267G>T
NM_001257990.2:c.76-267G>T
NG_016001.2:g.13911G>T
More... 		03/31/2019 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:FBXO7
Accession:NM_001033024
Location:INTRON

Gene Symbol:FBXO7
Accession:NM_001257990
Location:INTRON

Gene Symbol:FBXO7
Accession:NM_012179
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001688630 CLINVAR
dbSNP (RS) rs4820079 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene FBXO7 CLINVAR
OMIM 605648 CLINVAR