CLIC1 chloride intracellular channel 1

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Information
Clinical Significance
Ranking
Frequency
Disease area statistics
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Information

Symbol: CLIC1
Type: protein-coding
Description: chloride intracellular channel 1
Entrez Gene ID: 1192
Genome: hg19
Position: chr6:31,698,358-31,705,095
Genome: hg38
Position: chr6:31,730,581-31,737,318
MIM: 602872 OMIM
HGNC: HGNC:2062 HGNC
Ensembl: ENSG00000213719 Ensembl
Links: NCBI Gene Cards OncoKB

Clinical Significance

	MGeND	ClinVar
Likely benign	0	2
not provided	2	0
Uncertain significance	0	20

Ranking

	ClinVar
	0
	0
	0
	22
	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

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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	CL1C1
SYNONYM	CLCNL1
SYNONYM	G6
SYNONYM	NCC27
MIM	602872 OMIM
HGNC	HGNC:2062 HGNC
Ensembl	ENSG00000213719 Ensembl
AllianceGenome	HGNC:2062

Descrption	Source	Links

ID	Genome	Chromosome	Start	End	Length
ENST00000395892.5	hg38	chr6	31,730,581	31,739,763	9,183
ENST00000375779.6	hg38	chr6	31,730,581	31,736,572	5,992
ENST00000375780.6	hg38	chr6	31,730,581	31,737,318	6,738
ENST00000375784.8	hg38	chr6	31,730,599	31,736,530	5,932
ENST00000616760.1	hg38	chr6	31,730,583	31,736,545	5,963
ENST00000375779.6	hg19	chr6	31,698,358	31,704,349	5,992
ENST00000375780.6	hg19	chr6	31,698,358	31,705,095	6,738
ENST00000395892.5	hg19	chr6	31,698,358	31,707,540	9,183
ENST00000616760.1	hg19	chr6	31,698,360	31,704,322	5,963
ENST00000375784.8	hg19	chr6	31,698,376	31,704,307	5,932

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