RGD:26920476 Rat Genome Database

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Variant: RGD:26920476 -  Homo sapiens

RGD ID: 26920476
RS ID: rs1326404435
ClinVar ID: CV851609
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: BUB1B  LOC107984763  
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 15 40,494,603
GRCh38 15 40,202,402
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
LRG_489t1:c.1568-3T>C
NM_001211.6:c.1568-3T>C
LRG_489:g.46394T>C
NG_016338.1:g.46394T>C
More... 		12/11/2019 intron variant uncertain significance Warburton-Anyane-Yeboa syndrome
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:BUB1B
Accession:NM_001211
Location:INTRON

Gene Symbol:LOC107984763
Accession:XR_001751506
Location:INTRON;NON-CODING

Variant Samples
Additional References at PubMed
PMID:9536098   PMID:17576681   PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV002240382 CLINVAR
dbSNP (RS) rs1326404435 CLINVAR
MedGen C1850343 CLINVAR
NCBI Gene BUB1B CLINVAR
OMIM 257300 CLINVAR
  602860 CLINVAR