WRNIP1 WRN helicase interacting protein 1

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Information
Clinical Significance
Ranking
Frequency
Disease area statistics
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Information

Symbol: WRNIP1
Type: protein-coding
Description: WRN helicase interacting protein 1
Entrez Gene ID: 56897
Genome: hg19
Position: chr6:2,765,627-2,787,186
Genome: hg38
Position: chr6:2,765,393-2,786,952
MIM: 608196 OMIM
HGNC: HGNC:20876 HGNC
Ensembl: ENSG00000124535 Ensembl
Links: NCBI Gene Cards OncoKB

Clinical Significance

	MGeND	ClinVar
Benign	0	2
Likely benign	0	12
Uncertain significance	0	118

Ranking

	ClinVar
	0
	0
	0
	132
	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

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
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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	CFAP93
SYNONYM	FAP93
SYNONYM	WHIP
SYNONYM	bA420G6.2
MIM	608196 OMIM
HGNC	HGNC:20876 HGNC
Ensembl	ENSG00000124535 Ensembl
AllianceGenome	HGNC:20876

Descrption	Source	Links

ID	Genome	Chromosome	Start	End	Length
ENST00000618555.4	hg38	chr6	2,765,432	2,785,744	20,313
ENST00000380769.8	hg38	chr6	2,766,052	2,786,952	20,901
ENST00000380764.1	hg38	chr6	2,768,773	2,785,745	16,973
ENST00000380771.8	hg38	chr6	2,765,414	2,785,745	20,332
ENST00000380773.9	hg38	chr6	2,765,393	2,786,952	21,560
ENST00000380773.9	hg19	chr6	2,765,627	2,787,186	21,560
ENST00000380771.8	hg19	chr6	2,765,648	2,785,979	20,332
ENST00000618555.4	hg19	chr6	2,765,666	2,785,978	20,313
ENST00000380769.8	hg19	chr6	2,766,286	2,787,186	20,901
ENST00000380764.1	hg19	chr6	2,769,007	2,785,979	16,973

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