rs66481974 Rat Genome Database

rs66481974 Rat Genome Database

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Variant: rs66481974 - Homo sapiens

RGD ID:

11547384

RS ID:

rs66481974

ClinVar ID:

CV255887

Genic Status:

GENIC

Type:

SNV (SO:0001483)

Associated Genes:

MAF WWOX

Reference Nucleotide:

T

Variant Nucleotide:

C

Position

Assembly	Chr	Position
GRCh37	16	79,245,491
GRCh38	16	79,211,594

JBrowse:

View Region in Genome Browser (JBrowse)

Model

HGVS Name(s)	Last Evaluated	Molecular Consequence	Clinical Significance	Trait Synonyms
NG_011698.1:g.1116941T>C NC_000016.10:g.79211594T>C NC_000016.9:g.79245491T>C NM_016373.2:c.1057-14T>C More...	01/14/2016	intron variant	benign	AllHighlyPenetrant; Autosomal recessive spinocerebellar ataxia 12; Epileptic encephalopathy, early infantile, 1; Epileptic encephalopathy, early infantile, 28; INFANTILE SPASM SYNDROME, X-LINKED 1; none provided; OHTAHARA SYNDROME, X-LINKED; RECLASSIFIED - ADRA2C POLYMORPHISM; RECLASSIFIED - ADRB1 POLYMORPHISM; SPINOCEREBELLAR ATAXIA WITH MENTAL RETARDATION AND EPILEPSY; Tonic spasms with clustering, arrest of psychomotor development and hypsarrhythmia on EEG; West's syndrome; X-Linked Infantile Spasm Syndrome; X-linked infantile spasms

Object Symbol	Species	Term	Qualifier	Evidence	With	Reference	Notes	Source	Original Reference(s)
CV255887	Human	autosomal recessive spinocerebellar ataxia 12		IAGP		8554872	ClinVar Annotator: match by term: Autosomal recessive spinocerebellar ataxia 12	ClinVar	PMID:25741868\|PMID:28492532
CV255887	Human	developmental and epileptic encephalopathy 1		IAGP		8554872	ClinVar Annotator: match by term: Epileptic encephalopathy, early infantile, 1	ClinVar	PMID:25741868\|PMID:28492532
CV255887	Human	developmental and epileptic encephalopathy 28		IAGP		8554872	ClinVar Annotator: match by term: Developmental and epileptic encephalopathy, 28	ClinVar	PMID:25741868\|PMID:28492532

Gene Symbol:	MAF
Accession:	XM_024450279
Location:	3UTRS;EXON

Gene Symbol:	MAF
Accession:	XR_001751902
Location:	EXON;NON-CODING

Gene Symbol:	MAF
Accession:	XR_002957804
Location:	EXON;NON-CODING

Gene Symbol:	MAF
Accession:	XR_002957803
Location:	EXON;NON-CODING

Gene Symbol:	MAF
Accession:	XR_002957802
Location:	EXON;NON-CODING

Gene Symbol:	WWOX
Accession:	NM_016373
Location:	INTRON

Gene Symbol:	WWOX
Accession:	NM_130791
Location:	INTRON

Gene Symbol:	MAF
Accession:	NM_005360
Location:	INTRON

Gene Symbol:	MAF
Accession:	NM_001031804
Location:	INTRON

Gene Symbol:	WWOX
Accession:	NM_001291997
Location:	INTRON

Gene Symbol:	MAF
Accession:	XM_017023234
Location:	INTRON

Gene Symbol:	MAF
Accession:	XM_017023235
Location:	INTRON

Gene Symbol:	MAF
Accession:	XM_017023233
Location:	INTRON

Gene Symbol:	WWOX
Accession:	NR_120436
Location:	INTRON;NON-CODING

Gene Symbol:	WWOX
Accession:	NR_120435
Location:	INTRON;NON-CODING

ClinVar GRCh37	ClinVar GRCh38

PMID:25741868	PMID:28492532

Database	Acc Id	Source(s)
ClinVar	RCV000247690	CLINVAR
	RCV001515358	CLINVAR
	RCV002244634	CLINVAR
	RCV002244635	CLINVAR
	RCV004709463	CLINVAR
dbSNP (RS)	rs66481974	CLINVAR
MedGen	C3280452	CLINVAR
	C3463992	CLINVAR
	C3661900	CLINVAR
	C4015519	CLINVAR
	CN169374	CLINVAR
NCBI Gene	MAF	CLINVAR
	WWOX	CLINVAR
OMIM	177075	CLINVAR
	308350	CLINVAR
	605131	CLINVAR
	614322	CLINVAR
	616211	CLINVAR