CDH26 cadherin 26
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 10 |
Uncertain significance | 0 | 116 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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126 |
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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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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 | VR20 |
MIM | 617685 OMIM |
HGNC | HGNC:15902 HGNC |
Ensembl | ENSG00000124215 Ensembl |
AllianceGenome | HGNC:15902 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000244049.7 | hg38 | chr20 | 59,996,364 | 60,014,079 | 17,716 |
ENST00000348616.9 | hg38 | chr20 | 59,958,423 | 60,014,529 | 56,107 |
ENST00000350849.10 | hg38 | chr20 | 59,996,374 | 60,014,529 | 18,156 |
ENST00000348616.9 | hg19 | chr20 | 58,533,478 | 58,589,584 | 56,107 |
ENST00000244049.7 | hg19 | chr20 | 58,571,419 | 58,589,134 | 17,716 |
ENST00000350849.10 | hg19 | chr20 | 58,571,429 | 58,589,584 | 18,156 |
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