rs2275219 Rat Genome Database

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Variant: rs2275219 -  Homo sapiens

RGD ID: 150486696
RS ID: rs2275219
ClinVar ID: CV1283654
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: KIF11  
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 10 94,372,942
GRCh38 10 92,613,185
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.789+55T>C
NG_032580.1:g.25118T>C
NC_000010.11:g.92613185T>C
NC_000010.10:g.94372942T>C
 07/31/2018 intron variant benign none provided

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

Variant Samples
Additional References at PubMed
PMID:25741868  


Additional Information

Database Acc Id Source(s)
ClinVar RCV001715827 CLINVAR
dbSNP (RS) rs2275219 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene KIF11 CLINVAR
OMIM 148760 CLINVAR