TCP1 t-complex 1

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Information
Clinical Significance
Ranking
Frequency
Disease area statistics
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Information

Symbol: TCP1
Type: protein-coding
Description: t-complex 1
Entrez Gene ID: 6950
Genome: hg19
Position: chr6:160,199,530-160,210,634
Genome: hg38
Position: chr6:159,778,498-159,789,602
MIM: 186980 OMIM
HGNC: HGNC:11655 HGNC
Ensembl: ENSG00000120438 Ensembl
Links: NCBI Gene Cards OncoKB

Clinical Significance

	MGeND	ClinVar
Pathogenic	1	0
Likely benign	0	6
Uncertain significance	0	50

Ranking

	ClinVar
	0
	0
	0
	56
	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
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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	CCT-alpha
SYNONYM	CCT1
SYNONYM	CCTa
SYNONYM	D6S230E
SYNONYM	TCP-1-alpha
MIM	186980 OMIM
HGNC	HGNC:11655 HGNC
Ensembl	ENSG00000120438 Ensembl
AllianceGenome	HGNC:11655

Descrption	Source	Links

ID	Genome	Chromosome	Start	End	Length
ENST00000321394.12	hg38	chr6	159,778,498	159,789,602	11,105
ENST00000544255.5	hg38	chr6	159,778,964	159,789,596	10,633
ENST00000392168.6	hg38	chr6	159,778,987	159,789,703	10,717
ENST00000420894.6	hg38	chr6	159,778,985	159,789,572	10,588
ENST00000321394.12	hg19	chr6	160,199,530	160,210,634	11,105
ENST00000544255.5	hg19	chr6	160,199,996	160,210,628	10,633
ENST00000392168.6	hg19	chr6	160,200,019	160,210,735	10,717
ENST00000420894.6	hg19	chr6	160,200,017	160,210,604	10,588

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