RORC RAR related orphan receptor C

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Information
Clinical Significance
Ranking
Frequency
Disease area statistics
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Information

Symbol: RORC
Type: protein-coding
Description: RAR related orphan receptor C
Entrez Gene ID: 6097
Genome: hg19
Position: chr1:151,778,547-151,804,278
Genome: hg38
Position: chr1:151,806,071-151,831,802
MIM: 602943 OMIM
HGNC: HGNC:10260 HGNC
Ensembl: ENSG00000143365 Ensembl
Links: NCBI Gene Cards OncoKB

Clinical Significance

	MGeND	ClinVar
Pathogenic	0	10
Likely pathogenic	0	4
Benign	0	46
Likely benign	0	250
Conflicting classifications of pathogenicity	0	2
Uncertain significance	0	236

Ranking

	ClinVar
	0
	0
	54
	482
	6

Frequency

EXAC_EAS

EXAC_EAS

HGVD

HGVD

TOMMO

TOMMO

Gene

Position

EXAC_EAS

EXAC_EAS

HGVD

HGVD

TOMMO

TOMMO

Gene

Position

Disease area statistics

[No Data.]

Locus Zoom

Variants

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Target data	:	MGeND data only
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Variant name	Gene	AA change	CDS	Japanese frequency	TogoVar	MGeND				Genome	ClinVar			CIViC evidence	DisGeNET entry	COSMIC occurrence	Prediction
Variant name	Gene	AA change	CDS	Japanese frequency	TogoVar	Entry	Origin	Type	Annotation	Genome	Entry	Origin	Annotation	CIViC evidence	DisGeNET entry	COSMIC occurrence	Prediction

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Target data	:	MGeND data only
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Name	MGeND				Type	Genome	Size	Chromosome	Start	Stop	Ref	Alt	ClinVar	Origin	Entry	CIViC evidence	DisGeNET entry
Name	Entry	Origin	Type	Annotation	Type	Genome	Size	Chromosome	Start	Stop	Ref	Alt	ClinVar	Origin	Entry	CIViC evidence	DisGeNET entry

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Target data	:	MGeND data only
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Name	MGeND				Type	Genome	Gene symbol	Chromosome	Genomic start	Genomic stop	Strand	Ref	Alt	ClinVar	Origin	Entry	CIViC evidence	DisGeNET entry
Name	Entry	Origin	Type	Annotation	Type	Genome	Gene symbol	Chromosome	Genomic start	Genomic stop	Strand	Ref	Alt	ClinVar	Origin	Entry	CIViC evidence	DisGeNET entry

Type	ID
SYNONYM	IMD42
SYNONYM	NR1F3
SYNONYM	RORG
SYNONYM	RZR-GAMMA
SYNONYM	RZRG
SYNONYM	TOR
MIM	602943 OMIM
HGNC	HGNC:10260 HGNC
Ensembl	ENSG00000143365 Ensembl
AllianceGenome	HGNC:10260

Descrption	Source	Links

ID	Genome	Chromosome	Start	End	Length
ENST00000652040.2	hg38	chr1	151,806,120	151,831,845	25,726
ENST00000356728.11	hg38	chr1	151,806,071	151,826,096	20,026
ENST00000318247.7	hg38	chr1	151,806,071	151,831,802	25,732
ENST00000356728.11	hg19	chr1	151,778,547	151,798,572	20,026
ENST00000318247.7	hg19	chr1	151,778,547	151,804,278	25,732
ENST00000652040.2	hg19	chr1	151,778,596	151,804,321	25,726

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