rs183977797 Rat Genome Database

rs183977797 Rat Genome Database

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Variant: rs183977797 - Homo sapiens

RGD ID:

152096731

RS ID:

rs183977797

ClinVar ID:

CV1558029

Genic Status:

GENIC

Type:

SNV (SO:0001483)

Associated Genes:

MTO1

Reference Nucleotide:

G

Variant Nucleotide:

A

Position

Assembly	Chr	Position
GRCh37	6	74,207,631
GRCh38	6	73,497,908

JBrowse:

View Region in Genome Browser (JBrowse)

Model

HGVS Name(s)	Last Evaluated	Molecular Consequence	Clinical Significance	Trait Synonyms
NM_012123.4:c.1917+12G>A NM_133645.3:c.1992+12G>A NM_001123226.2:c.2037+12G>A NG_032856.2:g.41178G>A More...	08/16/2023	intron variant	likely benign	CARDIOMYOPATHY, INFANTILE HYPERTROPHIC MITOCHONDRIAL, AND LACTIC ACIDOSIS; Combined oxidative phosphorylation deficiency 10

Object Symbol	Species	Term	Qualifier	Evidence	With	Reference	Notes	Source	Original Reference(s)
CV1558029	Human	combined oxidative phosphorylation deficiency 10		IAGP		8554872	ClinVar Annotator: match by term: Mitochondrial hypertrophic cardiomyopathy with lactic acidosis due to MTO1 deficiency	ClinVar	PMID:28492532

Gene Symbol:	MTO1
Accession:	NM_133645
Location:	INTRON

Gene Symbol:	MTO1
Accession:	XM_047418606
Location:	INTRON

Gene Symbol:	MTO1
Accession:	NM_001123226
Location:	INTRON

Gene Symbol:	MTO1
Accession:	XM_047418605
Location:	INTRON

Gene Symbol:	MTO1
Accession:	NM_012123
Location:	INTRON

Gene Symbol:	MTO1
Accession:	XM_047418607
Location:	INTRON

ClinVar GRCh37	ClinVar GRCh38

PMID:28492532

Database	Acc Id	Source(s)
ClinVar	RCV002172557	CLINVAR
dbSNP (RS)	rs183977797	CLINVAR
MedGen	C4749921	CLINVAR
NCBI Gene	MTO1	CLINVAR
OMIM	614667	CLINVAR
	614702	CLINVAR