rs80320073 Rat Genome Database

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Variant: rs80320073 -  Homo sapiens

RGD ID: 150432953
RS ID: rs80320073
ClinVar ID: CV1203477
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: KIF11  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 10 94,404,823
GRCh38 10 92,645,066
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.2268-297C>T
NG_032580.1:g.56999C>T
NC_000010.11:g.92645066C>T
NC_000010.10:g.94404823C>T
 04/06/2019 intron variant likely 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 RCV001581632 CLINVAR
dbSNP (RS) rs80320073 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene KIF11 CLINVAR
OMIM 148760 CLINVAR