CDH3 cadherin 3
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Pathogenic | 0 | 56 |
Likely pathogenic | 0 | 38 |
Benign | 0 | 98 |
Likely benign | 0 | 538 |
Conflicting classifications of pathogenicity | 0 | 70 |
Uncertain significance | 0 | 702 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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190 |
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1,204 |
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16 |
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 |
---|---|
SYNONYM | CDHP |
SYNONYM | HJMD |
SYNONYM | PCAD |
MIM | 114021 OMIM |
HGNC | HGNC:1762 HGNC |
Ensembl | ENSG00000062038 Ensembl |
AllianceGenome | HGNC:1762 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000264012.9 | hg38 | chr16 | 68,645,310 | 68,700,292 | 54,983 |
ENST00000429102.6 | hg38 | chr16 | 68,644,993 | 68,699,036 | 54,044 |
ENST00000429102.6 | hg19 | chr16 | 68,678,896 | 68,732,939 | 54,044 |
ENST00000264012.9 | hg19 | chr16 | 68,679,213 | 68,734,195 | 54,983 |
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