RGD:407477020 Rat Genome Database

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Variant: RGD:407477020 -  Homo sapiens

RGD ID: 407477020
ClinVar ID: CV3417944
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: BUB1B  BUB1B-PAK6  
Reference Nucleotide: G
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 15 40,512,942
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
LRG_489t1:c.3135G>C
NM_001128629.3:c.-118+3074G>C
NM_001128628.3:c.-201+3074G>C
NM_001211.6:c.3135G>C
More... 		03/27/2024 intron variant likely benign
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV004604268 CLINVAR
MedGen C0950123 CLINVAR
NCBI Gene BUB1B CLINVAR
  BUB1B-PAK6 CLINVAR
OMIM 602860 CLINVAR