rs961367497 Rat Genome Database

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Variant: rs961367497 -  Homo sapiens

RGD ID: 152118677
RS ID: rs961367497
ClinVar ID: CV1659064
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: KIF11  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 10 94,410,282
GRCh38 10 92,650,525
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.3039+8A>G
NG_032580.1:g.62458A>G
NC_000010.11:g.92650525A>G
NC_000010.10:g.94410282A>G
 03/19/2022 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 RCV002175271 CLINVAR
dbSNP (RS) rs961367497 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene KIF11 CLINVAR
OMIM 148760 CLINVAR