RGD:407458238 Rat Genome Database

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Variant: RGD:407458238 -  Homo sapiens

RGD ID: 407458238
ClinVar ID: CV3455364
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: IRF8  
Reference Nucleotide: C
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 16 85,952,271
GRCh38 16 85,918,665
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
LRG_294t1:c.850C>G
NM_001363908.1:c.238C>G
NM_002163.4:c.850C>G
NM_001363907.1:c.880C>G
More...
05/01/2024 missense variant uncertain significance
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV004633197 CLINVAR
MedGen C0950123 CLINVAR
NCBI Gene IRF8 CLINVAR
OMIM 601565 CLINVAR