RGD:150506323 Rat Genome Database

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Variant: RGD:150506323 -  Homo sapiens

RGD ID: 150506323
RS ID: rs56340568
ClinVar ID: CV1213750
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: TALDO1  
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 11 758,806
GRCh38 11 758,806
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_006755.2:c.222-144C>T
NG_008160.1:g.16375C>T
NC_000011.10:g.758806C>T
NC_000011.9:g.758806C>T
 11/12/2018 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:TALDO1
Accession:NM_006755
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001596007 CLINVAR
dbSNP (RS) rs56340568 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene TALDO1 CLINVAR
OMIM 602063 CLINVAR