rs11818705 Rat Genome Database

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Variant: rs11818705 -  Homo sapiens

RGD ID: 150445172
RS ID: rs11818705
ClinVar ID: CV1215448
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: KIF11  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 10 94,392,728
GRCh38 10 92,632,971
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.1702+278C>T
NG_032580.1:g.44904C>T
NC_000010.11:g.92632971C>T
NC_000010.10:g.94392728C>T
 07/08/2018 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:KIF11
Accession:NM_004523
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001611041 CLINVAR
dbSNP (RS) rs11818705 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene KIF11 CLINVAR
OMIM 148760 CLINVAR