rs767310274 Rat Genome Database

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Variant: rs767310274 -  Homo sapiens

RGD ID: 152056140
RS ID: rs767310274
ClinVar ID: CV1591004
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: KIF11  
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 10 94,408,198
GRCh38 10 92,648,441
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.2770+7T>C
NG_032580.1:g.60374T>C
NC_000010.11:g.92648441T>C
NC_000010.10:g.94408198T>C
 08/04/2023 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 RCV002109564 CLINVAR
dbSNP (RS) rs767310274 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene KIF11 CLINVAR
OMIM 148760 CLINVAR