rs10786050 Rat Genome Database

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Variant: rs10786050 -  Homo sapiens

RGD ID: 150498270
RS ID: rs10786050
ClinVar ID: CV1255552
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: KIF11  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 10 94,367,230
GRCh38 10 92,607,473
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.387+236A>G
NG_032580.1:g.19406A>G
NC_000010.11:g.92607473A>G
NC_000010.10:g.94367230A>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 RCV001676339 CLINVAR
dbSNP (RS) rs10786050 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene KIF11 CLINVAR
OMIM 148760 CLINVAR