RGD:405282051 Rat Genome Database

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Variant: RGD:405282051 -  Homo sapiens

RGD ID: 405282051
ClinVar ID: CV3224722
Genic Status: GENIC
Type: deletion (SO:0000159) 
Associated Genes: WDR26  
Reference Nucleotide: GCTTCTTCT
Variant Nucleotide: -
Position
Assembly Chr Position
GRCh37 1 224,621,454 - 224,621,463
GRCh38 1 224,433,752 - 224,433,761
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001115113.3:c.347_355del
NM_025160.7:c.347_355del
NM_001379403.1:c.647_655del
NG_047198.1:g.5541_5549del
More... 		03/25/2024 inframe_deletion uncertain significance INTELLECTUAL DISABILITY WITH SEIZURES, ABNORMAL GAIT, AND DISTINCTIVE FACIAL FEATURES
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Samples
Additional References at PubMed
PMID:25741868  


Additional Information

Database Acc Id Source(s)
ClinVar RCV003989058 CLINVAR
MedGen C4539927 CLINVAR
NCBI Gene WDR26 CLINVAR
OMIM 617424 CLINVAR
  617616 CLINVAR