PHF10 PHD finger protein 10

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Information
Clinical Significance
Ranking
Frequency
Disease area statistics
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Information

Symbol: PHF10
Type: protein-coding
Description: PHD finger protein 10
Entrez Gene ID: 55274
Genome: hg19
Position: chr6:170,103,998-170,124,596
Genome: hg38
Position: chr6:169,703,902-169,724,500
MIM: 613069 OMIM
HGNC: HGNC:18250 HGNC
Ensembl: ENSG00000130024 Ensembl
Links: NCBI Gene Cards OncoKB

Clinical Significance

	MGeND	ClinVar
Benign	0	2
Likely benign	0	4
Uncertain significance	0	38

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

[No Data.]

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	BAF45A
SYNONYM	SMARCG4
SYNONYM	XAP135
MIM	613069 OMIM
HGNC	HGNC:18250 HGNC
Ensembl	ENSG00000130024 Ensembl
AllianceGenome	HGNC:18250

Descrption	Source	Links

ID	Genome	Chromosome	Start	End	Length
ENST00000366780.8	hg38	chr6	169,703,905	169,723,931	20,027
ENST00000612128.1	hg38	chr6	169,707,028	169,724,005	16,978
ENST00000621772.4	hg38	chr6	169,703,908	169,725,566	21,659
ENST00000339209.9	hg38	chr6	169,703,902	169,724,500	20,599
ENST00000339209.9	hg19	chr6	170,103,998	170,124,596	20,599
ENST00000366780.8	hg19	chr6	170,104,001	170,124,027	20,027
ENST00000621772.4	hg19	chr6	170,104,004	170,125,662	21,659
ENST00000612128.1	hg19	chr6	170,107,124	170,124,101	16,978

Key	Value
strand	-
start	170,104,001
Gene Symbol	PHF10
Entrez GeneId	55,274
Chr Band	6q27
end	170,124,105
chr	chr6

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