IFI27 interferon alpha inducible protein 27

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Information
Clinical Significance
Ranking
Frequency
Disease area statistics
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Information

Symbol: IFI27
Type: protein-coding
Description: interferon alpha inducible protein 27
Entrez Gene ID: 3429
Genome: hg19
Position: chr14:94,577,161-94,583,032
Genome: hg38
Position: chr14:94,110,815-94,116,695
MIM: 600009 OMIM
HGNC: HGNC:5397 HGNC
Ensembl: ENSG00000165949 Ensembl
Links: NCBI Gene Cards OncoKB

Clinical Significance

	MGeND	ClinVar
Benign	0	2
Likely benign	0	2
Uncertain significance	0	10

Ranking

	ClinVar
	0
	0
	0
	14
	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

[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

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	FAM14D
SYNONYM	ISG12
SYNONYM	ISG12A
SYNONYM	P27
MIM	600009 OMIM
HGNC	HGNC:5397 HGNC
Ensembl	ENSG00000165949 Ensembl
AllianceGenome	HGNC:5397

Descrption	Source	Links

ID	Genome	Chromosome	Start	End	Length
ENST00000612813.4	hg38	chr14	94,110,815	94,116,695	5,881
ENST00000621160.5	hg38	chr14	94,110,736	94,116,690	5,955
ENST00000620396.4	hg38	chr14	94,110,762	94,116,693	5,932
ENST00000618863.1	hg38	chr14	94,110,734	94,116,690	5,957
ENST00000618863.1	hg19	chr14	94,577,080	94,583,027	5,948
ENST00000621160.5	hg19	chr14	94,577,082	94,583,027	5,946
ENST00000620396.4	hg19	chr14	94,577,108	94,583,030	5,923
ENST00000612813.4	hg19	chr14	94,577,161	94,583,032	5,872

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