rs756032812 Rat Genome Database

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Variant: rs756032812 -  Homo sapiens

RGD ID: 127281875
RS ID: rs756032812
ClinVar ID: CV1077630
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: KIF11  
Reference Nucleotide: T
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 10 94,366,360
GRCh38 10 92,606,603
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.211-16T>A
NG_032580.1:g.18536T>A
NC_000010.11:g.92606603T>A
NC_000010.10:g.94366360T>A
 07/07/2023 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 RCV001410735 CLINVAR
dbSNP (RS) rs756032812 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene KIF11 CLINVAR
OMIM 148760 CLINVAR