rs141960153 Rat Genome Database

rs141960153 Rat Genome Database

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Variant: rs141960153 - Homo sapiens

RGD ID:

150465513

RS ID:

rs141960153

ClinVar ID:

CV1201088

Genic Status:

GENIC

Type:

SNV (SO:0001483)

Associated Genes:

Reference Nucleotide:

A

Variant Nucleotide:

G

Position

Assembly	Chr	Position
GRCh37	6	158,535,653
GRCh38	6	158,114,621

JBrowse:

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Model

HGVS Name(s)	Last Evaluated	Molecular Consequence	Clinical Significance	Trait Synonyms
NM_032861.4:c.1684+168T>C NG_032889.1:g.58660T>C NC_000006.12:g.158114621A>G NC_000006.11:g.158535653A>G NR_073096.2:n.1767T>C More...	07/09/2018	intron variant	likely benign	3-METHYLGLUTACONIC ACIDURIA, TYPE VI; MEGDEL syndrome; none provided; RECLASSIFIED - ADRA2C POLYMORPHISM; RECLASSIFIED - ADRB1 POLYMORPHISM

Object Symbol	Species	Term	Qualifier	Evidence	With	Reference	Notes	Source	Original Reference(s)
CV1201088	Human	3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome		IAGP		8554872	ClinVar Annotator: match by term: 3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome	ClinVar	PMID:25741868

Gene Symbol:	SERAC1
Accession:	NR_073096
Location:	EXON;NON-CODING

Gene Symbol:	SERAC1
Accession:	NM_032861
Location:	INTRON

Gene Symbol:	SERAC1
Accession:	XM_006715586
Location:	INTRON

Gene Symbol:	SERAC1
Accession:	XM_011536198
Location:	INTRON

Gene Symbol:	SERAC1
Accession:	XM_024446573
Location:	INTRON

Gene Symbol:	SERAC1
Accession:	XM_047419421
Location:	INTRON

Gene Symbol:	SERAC1
Accession:	XR_007059349
Location:	INTRON;NON-CODING

ClinVar GRCh37	ClinVar GRCh38

PMID:25741868

Database	Acc Id	Source(s)
ClinVar	RCV001587568	CLINVAR
	RCV002495928	CLINVAR
dbSNP (RS)	rs141960153	CLINVAR
MedGen	C3661900	CLINVAR
	C4040739	CLINVAR
NCBI Gene	SERAC1	CLINVAR
OMIM	614725	CLINVAR
	614739	CLINVAR