RFC4 replication factor C subunit 4

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Information
Clinical Significance
Ranking
Frequency
Disease area statistics
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Information

Symbol: RFC4
Type: protein-coding
Description: replication factor C subunit 4
Entrez Gene ID: 5984
Genome: hg19
Position: chr3:186,507,689-186,524,271
Genome: hg38
Position: chr3:186,789,900-186,806,482
MIM: 102577 OMIM
HGNC: HGNC:9972 HGNC
Ensembl: ENSG00000163918 Ensembl
Links: NCBI Gene Cards OncoKB

Clinical Significance

	MGeND	ClinVar
Likely pathogenic	1	0
Benign	0	2
Likely benign	0	2
not provided	2	0
Uncertain significance	0	40

Ranking

	ClinVar
	0
	0
	0
	44
	0

Frequency

EXAC_EAS

EXAC_EAS

HGVD

HGVD

TOMMO

TOMMO

Gene

Position

EXAC_EAS

EXAC_EAS

HGVD

HGVD

TOMMO

TOMMO

Gene

Position

Disease area statistics

Locus Zoom

Variants

Search Word

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

Search Word

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

Search Word

Target data	:	MGeND data only
Category	:
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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	A1
SYNONYM	RFC37
MIM	102577 OMIM
HGNC	HGNC:9972 HGNC
Ensembl	ENSG00000163918 Ensembl
AllianceGenome	HGNC:9972

Descrption	Source	Links

ID	Genome	Chromosome	Start	End	Length
ENST00000433496.5	hg38	chr3	186,789,880	186,804,724	14,845
ENST00000296273.7	hg38	chr3	186,789,900	186,806,482	16,583
ENST00000433496.5	hg19	chr3	186,507,669	186,522,513	14,845
ENST00000296273.7	hg19	chr3	186,507,689	186,524,271	16,583

Key	Value
strand	-
start	186,507,681
Gene Symbol	RFC4
Entrez GeneId	5,984
Chr Band	3q27
end	186,524,483
chr	chr3

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