CBLL1 Cbl proto-oncogene like 1
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Uncertain significance | 0 | 24 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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24 |
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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 | |||||
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Entry | Origin | Type | Annotation | Entry | Origin | Annotation |
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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 | |||
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Entry | Origin | Type | Annotation |
Search Word
Target data | : |
MGeND data only
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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 | |||
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Entry | Origin | Type | Annotation |
Type | ID |
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SYNONYM | HAKAI |
SYNONYM | RNF188 |
MIM | 606872 OMIM |
HGNC | HGNC:21225 HGNC |
Ensembl | ENSG00000105879 Ensembl |
AllianceGenome | HGNC:21225 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000440859.8 | hg38 | chr7 | 107,744,142 | 107,761,667 | 17,526 |
ENST00000698938.1 | hg38 | chr7 | 107,743,073 | 107,761,667 | 18,595 |
ENST00000415884.6 | hg38 | chr7 | 107,744,155 | 107,758,571 | 14,417 |
ENST00000222597.7 | hg38 | chr7 | 107,743,799 | 107,759,686 | 15,888 |
ENST00000698938.1 | hg19 | chr7 | 107,383,518 | 107,402,112 | 18,595 |
ENST00000222597.7 | hg19 | chr7 | 107,384,244 | 107,400,131 | 15,888 |
ENST00000440859.8 | hg19 | chr7 | 107,384,587 | 107,402,112 | 17,526 |
ENST00000415884.6 | hg19 | chr7 | 107,384,600 | 107,399,016 | 14,417 |
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