RGD:405243781 Rat Genome Database

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Variant: RGD:405243781 -  Homo sapiens

RGD ID: 405243781
ClinVar ID: CV3164827
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: TALDO1  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 11 764,269
GRCh38 11 764,269
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_006755.2:c.836-19G>A
NG_008160.1:g.21838G>A
NC_000011.10:g.764269G>A
NC_000011.9:g.764269G>A
 01/13/2023 intron variant likely benign none provided; RECLASSIFIED - ADRA2C POLYMORPHISM; RECLASSIFIED - ADRB1 POLYMORPHISM

Gene Symbol:TALDO1
Accession:NM_006755
Location:INTRON

.
PMID:28492532  



Database
Acc Id
Source(s)
ClinVar RCV003867908 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene TALDO1 CLINVAR
OMIM 602063 CLINVAR