RGD:156399612 Rat Genome Database

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Variant: RGD:156399612 -  Homo sapiens

RGD ID: 156399612
ClinVar ID: CV1984979
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: KIF11  
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 10 94,368,763
GRCh38 10 92,609,006
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_004523.4:c.388-14T>C
NG_032580.1:g.20939T>C
NC_000010.11:g.92609006T>C
NC_000010.10:g.94368763T>C
 06/04/2022 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:KIF11
Accession:NM_004523
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV002605474 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene KIF11 CLINVAR
OMIM 148760 CLINVAR