RGD:15150345 Rat Genome Database

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Variant: RGD:15150345 -  Homo sapiens

RGD ID: 15150345
RS ID: rs111358777
ClinVar ID: CV778800
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: KIF21B  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 1 200,974,670
GRCh38 1 201,005,542
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001252100.2:c.597+3G>A
NM_001252102.2:c.597+3G>A
NM_001252103.2:c.597+3G>A
NM_017596.4:c.597+3G>A
More... 		12/31/2019 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:KIF21B
Accession:NM_017596
Location:INTRON

Gene Symbol:KIF21B
Accession:NM_001252103
Location:INTRON

Gene Symbol:KIF21B
Accession:NM_001252100
Location:INTRON

Gene Symbol:KIF21B
Accession:XM_047449818
Location:INTRON

Gene Symbol:KIF21B
Accession:NM_001252102
Location:INTRON

Gene Symbol:KIF21B
Accession:XM_017000731
Location:INTRON

Gene Symbol:KIF21B
Accession:XM_017000732
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV000967927 CLINVAR
dbSNP (RS) rs111358777 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene KIF21B CLINVAR
OMIM 608322 CLINVAR