rs2135914686 Rat Genome Database

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Variant: rs2135914686 -  Homo sapiens

RGD ID: 127324352
RS ID: rs2135914686
ClinVar ID: CV1120844
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: KIF11  
Reference Nucleotide: C
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 10 94,390,130
GRCh38 10 92,630,373
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.1494+9C>A
NG_032580.1:g.42306C>A
NC_000010.11:g.92630373C>A
NC_000010.10:g.94390130C>A
 08/14/2019 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 RCV001468186 CLINVAR
dbSNP (RS) rs2135914686 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene KIF11 CLINVAR
OMIM 148760 CLINVAR