PRMT1 protein arginine methyltransferase 1

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Information
Clinical Significance
Ranking
Frequency
Disease area statistics
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Information

Symbol: PRMT1
Type: protein-coding
Description: protein arginine methyltransferase 1
Entrez Gene ID: 3276
Genome: hg19
Position: chr19:50,180,528-50,191,704
Genome: hg38
Position: chr19:49,677,271-49,688,447
MIM: 602950 OMIM
HGNC: HGNC:5187 HGNC
Ensembl: ENSG00000126457 Ensembl
Links: NCBI Gene Cards OncoKB

Clinical Significance

	MGeND	ClinVar
Benign	0	4
Likely benign	0	2
Uncertain significance	0	22

Ranking

	ClinVar
	0
	0
	0
	28
	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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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	ANM1
SYNONYM	HCP1
SYNONYM	HRMT1L2
SYNONYM	IR1B4
MIM	602950 OMIM
HGNC	HGNC:5187 HGNC
Ensembl	ENSG00000126457 Ensembl
AllianceGenome	HGNC:5187

Descrption	Source	Links

ID	Genome	Chromosome	Start	End	Length
ENST00000454376.7	hg38	chr19	49,677,271	49,688,447	11,177
ENST00000610806.4	hg38	chr19	49,677,152	49,688,450	11,299
ENST00000532489.5	hg38	chr19	49,675,897	49,688,447	12,551
ENST00000391851.8	hg38	chr19	49,677,152	49,688,447	11,296
ENST00000391851.8	hg19	chr19	50,180,409	50,191,704	11,296
ENST00000454376.7	hg19	chr19	50,180,528	50,191,704	11,177
ENST00000532489.5	hg19	chr19	50,179,154	50,191,704	12,551
ENST00000610806.4	hg19	chr19	50,180,409	50,191,707	11,299

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