CLEC1B C-type lectin domain family 1 member B
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Uncertain significance | 0 | 56 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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56 |
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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
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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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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 | 1810061I13Rik |
SYNONYM | CLEC2 |
SYNONYM | CLEC2B |
SYNONYM | PRO1384 |
SYNONYM | QDED721 |
MIM | 606783 OMIM |
HGNC | HGNC:24356 HGNC |
Ensembl | ENSG00000165682 Ensembl |
AllianceGenome | HGNC:24356 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000298527.11 | hg38 | chr12 | 9,993,075 | 9,999,121 | 6,047 |
ENST00000348658.4 | hg38 | chr12 | 9,993,065 | 9,999,300 | 6,236 |
ENST00000428126.6 | hg38 | chr12 | 9,990,950 | 10,013,424 | 22,475 |
ENST00000428126.6 | hg19 | chr12 | 10,143,549 | 10,166,023 | 22,475 |
ENST00000348658.4 | hg19 | chr12 | 10,145,664 | 10,151,899 | 6,236 |
ENST00000298527.11 | hg19 | chr12 | 10,145,674 | 10,151,720 | 6,047 |
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