rs17875339 Rat Genome Database

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Variant: rs17875339 -  Homo sapiens

RGD ID: 126755716
RS ID: rs17875339
ClinVar ID: CV994117
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: KIF11  
Reference Nucleotide: C
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 10 94,381,133
GRCh38 10 92,621,376
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.1129-9C>G
NG_032580.1:g.33309C>G
NC_000010.11:g.92621376C>G
NC_000010.10:g.94381133C>G
 03/10/2022 intron variant likely benign|uncertain significance none provided

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

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV001298415 CLINVAR
dbSNP (RS) rs17875339 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene KIF11 CLINVAR
OMIM 148760 CLINVAR