RGD:156123540 Rat Genome Database

RGD:156123540 Rat Genome Database

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Variant: RGD:156123540 - Homo sapiens

RGD ID:

156123540

ClinVar ID:

CV2039983

Genic Status:

GENIC

Type:

SNV (SO:0001483)

Associated Genes:

LOC126861110 TALDO1

Reference Nucleotide:

C

Variant Nucleotide:

T

Position

Assembly	Chr	Position
GRCh37	11	763,504
GRCh38	11	763,504

JBrowse:

View Region in Genome Browser (JBrowse)

Model

HGVS Name(s)	Last Evaluated	Molecular Consequence	Clinical Significance	Trait Synonyms
NM_006755.2:c.622C>T NG_085609.1:g.1017C>T NG_008160.1:g.21073C>T NC_000011.10:g.763504C>T More...	04/16/2022	missense variant	uncertain significance	none provided; RECLASSIFIED - ADRA2C POLYMORPHISM; RECLASSIFIED - ADRB1 POLYMORPHISM

Gene Symbol:	TALDO1
Accession:	NM_006755
Location:	EXON
Amino Acid Prediction:	P to S (nonsynonymous)
Amino Acid Position:	208

Amino Acid Sequence (Calculated using NCBI transcript definition)
MSSSPVKRQRMESALDQLKQFTTVVADTGDFHAIDEYKPQDATTNPSLILAAAQMPAYQELVEEAIAYGRKLGGSQEDQI KNAIDKLFVLFGAEILKKIPGRVSTEVDARLSFDKDAMVARARRLIELYKEAGISKDRILIKLSSTWEGIQAGKELEEQH GIHCNMTLLFSFAQAVACAEAGVTLISPFVGRILDWHVANTDKKSYESLEDPGVKSVTKIYNYYKKFSYKTIVMGASFRN TGEIKALAGCDFLTISPKLLGELLQDNAKLVPVLSAKAAQASDLEKIHLDEKSFRWLHNEDQMAVEKLSDGIRKFAADAV KLERMLTERMFNAENGK*

ClinVar GRCh37	ClinVar GRCh38

PMID:28492532

Database	Acc Id	Source(s)
ClinVar	RCV002785885	CLINVAR
MedGen	C3661900	CLINVAR
NCBI Gene	LOC126861110	CLINVAR
	TALDO1	CLINVAR
OMIM	602063	CLINVAR