RGD:150489777 Rat Genome Database

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Variant: RGD:150489777 -  Homo sapiens

RGD ID: 150489777
RS ID: rs41280563
ClinVar ID: CV1239005
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: SBF1  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 22 50,906,581
GRCh38 22 50,468,152
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001365819.1:c.141+224T>C
NM_002972.4:c.141+224T>C
NG_041810.1:g.11920T>C
NC_000022.11:g.50468152A>G
More... 		07/15/2018 intron variant benign none provided

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

Gene Symbol:
Accession:
Location:INTRON

Gene Symbol:SBF1
Accession:NM_001410794
Location:INTRON

Gene Symbol:SBF1
Accession:NM_001410795
Location:INTRON

Gene Symbol:SBF1
Accession:NM_002972
Location:INTRON

Gene Symbol:SBF1
Accession:NM_001365819
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001654573 CLINVAR
dbSNP (RS) rs41280563 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene SBF1 CLINVAR
OMIM 603560 CLINVAR