CLCF1 cardiotrophin like cytokine factor 1
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Pathogenic | 0 | 8 |
Benign | 0 | 2 |
Likely benign | 0 | 16 |
Uncertain significance | 0 | 30 |
Ranking
ClinVar | |
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0 |
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0 |
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8 |
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40 |
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8 |
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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Variant name | Gene | AA change | CDS | Japanese frequency |
TogoVar | MGeND | Genome | ClinVar | CIViC evidence | DisGeNET entry | COSMIC occurrence |
Prediction | |||||
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Entry | Origin | Type | Annotation | Entry | Origin | Annotation |
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MGeND data only
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Name | MGeND | Type | Genome | Size | Chromosome | Start | Stop | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
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Entry | Origin | Type | Annotation |
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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 | |||
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Entry | Origin | Type | Annotation |
Type | ID |
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SYNONYM | BSF-3 |
SYNONYM | BSF3 |
SYNONYM | CISS2 |
SYNONYM | CLC |
SYNONYM | NNT-1 |
SYNONYM | NNT1 |
SYNONYM | NR6 |
MIM | 607672 OMIM |
HGNC | HGNC:17412 HGNC |
Ensembl | ENSG00000175505 Ensembl |
AllianceGenome | HGNC:17412 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000533438.1 | hg38 | chr11 | 67,364,962 | 67,374,177 | 9,216 |
ENST00000312438.8 | hg38 | chr11 | 67,364,168 | 67,373,598 | 9,431 |
ENST00000312438.8 | hg19 | chr11 | 67,131,639 | 67,141,069 | 9,431 |
ENST00000533438.1 | hg19 | chr11 | 67,132,433 | 67,141,648 | 9,216 |
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