SINHCAF SIN3-HDAC complex associated factor

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Information
Clinical Significance
Ranking
Frequency
Disease area statistics
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Information

Symbol: SINHCAF
Type: protein-coding
Description: SIN3-HDAC complex associated factor
Entrez Gene ID: 58516
Genome: hg19
Position: chr12:31,433,518-31,479,084
Genome: hg38
Position: chr12:31,280,584-31,326,150
MIM: 615027 OMIM
HGNC: HGNC:30702 HGNC
Ensembl: ENSG00000139146 Ensembl
Links: NCBI Gene Cards OncoKB

Clinical Significance

	MGeND	ClinVar
Likely benign	0	4
Uncertain significance	0	8

Ranking

	ClinVar
	0
	0
	0
	12
	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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Filtering	:

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	C12orf14
SYNONYM	FAM60A
SYNONYM	L4
SYNONYM	TERA
MIM	615027 OMIM
HGNC	HGNC:30702 HGNC
Ensembl	ENSG00000139146 Ensembl
AllianceGenome	HGNC:30702

Descrption	Source	Links

ID	Genome	Chromosome	Start	End	Length
ENST00000337682.9	hg38	chr12	31,280,584	31,326,150	45,567
ENST00000539409.5	hg38	chr12	31,280,584	31,326,116	45,533
ENST00000454658.6	hg38	chr12	31,282,062	31,324,162	42,101
ENST00000542983.1	hg38	chr12	31,282,688	31,326,199	43,512
ENST00000539409.5	hg19	chr12	31,433,518	31,479,050	45,533
ENST00000337682.9	hg19	chr12	31,433,518	31,479,084	45,567
ENST00000454658.6	hg19	chr12	31,434,996	31,477,096	42,101
ENST00000542983.1	hg19	chr12	31,435,622	31,479,133	43,512

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