RGD:156029966 Rat Genome Database

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Variant: RGD:156029966 -  Homo sapiens

RGD ID: 156029966
ClinVar ID: CV2105458
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: LOC126861110  TALDO1  
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 11 763,500
GRCh38 11 763,500
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NP_006746.1:p.Tyr206=
NM_006755.2:c.618T>C
NG_085609.1:g.1013T>C
NG_008160.1:g.21069T>C
More... 		12/23/2021 synonymous variant likely benign none provided; RECLASSIFIED - ADRA2C POLYMORPHISM; RECLASSIFIED - ADRB1 POLYMORPHISM

Gene Symbol:TALDO1
Accession:NM_006755
Location:EXON
Amino Acid Prediction: Y to Y (synonymous)
Amino Acid Position: 206
Amino Acid Sequence
(Calculated using NCBI transcript definition)
MSSSPVKRQRMESALDQLKQFTTVVADTGDFHAIDEYKPQDATTNPSLILAAAQMPAYQELVEEAIAYGRKLGGSQEDQI
KNAIDKLFVLFGAEILKKIPGRVSTEVDARLSFDKDAMVARARRLIELYKEAGISKDRILIKLSSTWEGIQAGKELEEQH
GIHCNMTLLFSFAQAVACAEAGVTLISPFVGRILDWHVANTDKKSYEPLEDPGVKSVTKIYNYYKKFSYKTIVMGASFRN
TGEIKALAGCDFLTISPKLLGELLQDNAKLVPVLSAKAAQASDLEKIHLDEKSFRWLHNEDQMAVEKLSDGIRKFAADAV
KLERMLTERMFNAENGK*
.
PMID:28492532  



Database
Acc Id
Source(s)
ClinVar RCV002910021 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene LOC126861110 CLINVAR
  TALDO1 CLINVAR
OMIM 602063 CLINVAR