RGD:156278525 Rat Genome Database

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Variant: RGD:156278525 -  Homo sapiens

RGD ID: 156278525
ClinVar ID: CV2011447
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: TALDO1  
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 11 760,188
GRCh38 11 760,188
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_006755.2:c.396T>C
NG_008160.1:g.17757T>C
NC_000011.10:g.760188T>C
NC_000011.9:g.760188T>C
More... 		04/27/2023 synonymous variant likely benign none provided; RECLASSIFIED - ADRA2C POLYMORPHISM; RECLASSIFIED - ADRB1 POLYMORPHISM

Gene Symbol:TALDO1
Accession:NM_006755
Location:EXON
Amino Acid Prediction: A to A (synonymous)
Amino Acid Position: 132
Amino Acid Sequence
(Calculated using NCBI transcript definition)
MSSSPVKRQRMESALDQLKQFTTVVADTGDFHAIDEYKPQDATTNPSLILAAAQMPAYQELVEEAIAYGRKLGGSQEDQI
KNAIDKLFVLFGAEILKKIPGRVSTEVDARLSFDKDAMVARARRLIELYKEAGISKDRILIKLSSTWEGIQAGKELEEQH
GIHCNMTLLFSFAQAVACAEAGVTLISPFVGRILDWHVANTDKKSYEPLEDPGVKSVTKIYNYYKKFSYKTIVMGASFRN
TGEIKALAGCDFLTISPKLLGELLQDNAKLVPVLSAKAAQASDLEKIHLDEKSFRWLHNEDQMAVEKLSDGIRKFAADAV
KLERMLTERMFNAENGK*
.
PMID:28492532  



Database
Acc Id
Source(s)
ClinVar RCV002715220 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene TALDO1 CLINVAR
OMIM 602063 CLINVAR