CALB2 calbindin 2
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 4 |
Uncertain significance | 0 | 30 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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34 |
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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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Variant name | Gene | AA change | CDS | Japanese frequency |
TogoVar | MGeND | Genome | ClinVar | CIViC evidence | DisGeNET entry | COSMIC occurrence |
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Entry | Origin | Type | Annotation | Entry | Origin | Annotation |
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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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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 | CAB29 |
SYNONYM | CAL2 |
SYNONYM | CR |
MIM | 114051 OMIM |
HGNC | HGNC:1435 HGNC |
Ensembl | ENSG00000172137 Ensembl |
AllianceGenome | HGNC:1435 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000349553.9 | hg38 | chr16 | 71,358,713 | 71,390,436 | 31,724 |
ENST00000302628.9 | hg38 | chr16 | 71,358,723 | 71,390,433 | 31,711 |
ENST00000349553.9 | hg19 | chr16 | 71,392,616 | 71,424,339 | 31,724 |
ENST00000302628.9 | hg19 | chr16 | 71,392,626 | 71,424,336 | 31,711 |
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