RGD:156321962 Rat Genome Database

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Variant: RGD:156321962 -  Homo sapiens

RGD ID: 156321962
ClinVar ID: CV2067644
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: KIF11  
Reference Nucleotide: C
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 10 94,388,554
GRCh38 10 92,628,797
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.1218-11C>G
NG_032580.1:g.40730C>G
NC_000010.11:g.92628797C>G
NC_000010.10:g.94388554C>G
 07/03/2022 intron variant uncertain significance 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 RCV002834761 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene KIF11 CLINVAR
OMIM 148760 CLINVAR