rs145088125 Rat Genome Database

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Variant: rs145088125 -  Homo sapiens

RGD ID: 150499989
RS ID: rs145088125
ClinVar ID: CV1235832
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: KIF11  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 10 94,388,841
GRCh38 10 92,629,084
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.1305+189G>A
NG_032580.1:g.41017G>A
NC_000010.11:g.92629084G>A
NC_000010.10:g.94388841G>A
 07/17/2018 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 RCV001656515 CLINVAR
dbSNP (RS) rs145088125 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene KIF11 CLINVAR
OMIM 148760 CLINVAR