rs201855399 Rat Genome Database

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Variant: rs201855399 -  Homo sapiens

RGD ID: 151777393
RS ID: rs201855399
ClinVar ID: CV1381932
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: LOC126861110  TALDO1  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 11 763,424
GRCh38 11 763,424
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_006755.2:c.542C>T
NG_008160.1:g.20993C>T
NC_000011.10:g.763424C>T
NC_000011.9:g.763424C>T
More... 		09/06/2022 missense variant uncertain significance none provided

Gene Symbol:TALDO1
Accession:NM_006755
Location:EXON
Amino Acid Prediction: A to V (nonsynonymous)
Amino Acid Position: 181
Amino Acid Sequence
(Calculated using NCBI transcript definition)
MSSSPVKRQRMESALDQLKQFTTVVADTGDFHAIDEYKPQDATTNPSLILAAAQMPAYQELVEEAIAYGRKLGGSQEDQI
KNAIDKLFVLFGAEILKKIPGRVSTEVDARLSFDKDAMVARARRLIELYKEAGISKDRILIKLSSTWEGIQAGKELEEQH
GIHCNMTLLFSFAQAVACAEVGVTLISPFVGRILDWHVANTDKKSYEPLEDPGVKSVTKIYNYYKKFSYKTIVMGASFRN
TGEIKALAGCDFLTISPKLLGELLQDNAKLVPVLSAKAAQASDLEKIHLDEKSFRWLHNEDQMAVEKLSDGIRKFAADAV
KLERMLTERMFNAENGK*
.
PMID:28492532  



Database
Acc Id
Source(s)
ClinVar RCV001950740 CLINVAR
dbSNP (RS) rs201855399 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene LOC126861110 CLINVAR
  TALDO1 CLINVAR
OMIM 602063 CLINVAR