rs11816962 Rat Genome Database

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Variant: rs11816962 -  Homo sapiens

RGD ID: 150475480
RS ID: rs11816962
ClinVar ID: CV1271198
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: KIF11  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 10 94,396,614
GRCh38 10 92,636,857
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.1876-327A>G
NG_032580.1:g.48790A>G
NC_000010.11:g.92636857A>G
NC_000010.10:g.94396614A>G
 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 RCV001696021 CLINVAR
dbSNP (RS) rs11816962 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene KIF11 CLINVAR
OMIM 148760 CLINVAR