PRRG1 proline rich and Gla domain 1

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Information
Clinical Significance
Ranking
Frequency
Disease area statistics
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Information

Symbol: PRRG1
Type: protein-coding
Description: proline rich and Gla domain 1
Entrez Gene ID: 5638
Genome: hg19
Position: chrX:37,208,625-37,316,542
Genome: hg38
Position: chrX:37,349,372-37,457,289
MIM: 300935 OMIM
HGNC: HGNC:9469 HGNC
Ensembl: ENSG00000130962 Ensembl
Links: NCBI Gene Cards OncoKB

Clinical Significance

	MGeND	ClinVar
Likely benign	0	4
not provided	6	0
Uncertain significance	0	16

Ranking

	ClinVar
	0
	0
	0
	20
	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

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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
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	PRGP1
MIM	300935 OMIM
HGNC	HGNC:9469 HGNC
Ensembl	ENSG00000130962 Ensembl
AllianceGenome	HGNC:9469

Descrption	Source	Links

ID	Genome	Chromosome	Start	End	Length
ENST00000463135.1	hg38	chrX	37,349,379	37,442,224	92,846
ENST00000542554.5	hg38	chrX	37,349,330	37,457,292	107,963
ENST00000449135.6	hg38	chrX	37,349,372	37,457,289	107,918
ENST00000378628.9	hg38	chrX	37,349,364	37,457,291	107,928
ENST00000543642.5	hg38	chrX	37,349,330	37,457,292	107,963
ENST00000542554.5	hg19	chrX	37,208,583	37,316,545	107,963
ENST00000543642.5	hg19	chrX	37,208,583	37,316,545	107,963
ENST00000378628.9	hg19	chrX	37,208,617	37,316,544	107,928
ENST00000449135.6	hg19	chrX	37,208,625	37,316,542	107,918
ENST00000463135.1	hg19	chrX	37,208,632	37,301,477	92,846

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