RGD:150515484 Rat Genome Database

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Variant: RGD:150515484 -  Homo sapiens

RGD ID: 150515484
RS ID: rs3761435
ClinVar ID: CV1227572
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: LOC127895927  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 22 32,870,574
GRCh38 22 32,474,587
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Clinical Significance Trait Synonyms
NG_016001.2:g.4868A>G
NC_000022.11:g.32474587A>G
NC_000022.10:g.32870574A>G
 07/05/2018 benign none provided

Variant Details
Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001638846 CLINVAR
dbSNP (RS) rs3761435 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene FBXO7 CLINVAR
OMIM 605648 CLINVAR