CDH7 cadherin 7
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 72 |
Likely benign | 0 | 4 |
Uncertain significance | 0 | 76 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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2 |
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150 |
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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 | CDH7L1 |
MIM | 605806 OMIM |
HGNC | HGNC:1766 HGNC |
Ensembl | ENSG00000081138 Ensembl |
AllianceGenome | HGNC:1766 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000536984.6 | hg38 | chr18 | 65,750,653 | 65,864,125 | 113,473 |
ENST00000323011.7 | hg38 | chr18 | 65,750,252 | 65,880,939 | 130,688 |
ENST00000397968.4 | hg38 | chr18 | 65,751,012 | 65,890,337 | 139,326 |
ENST00000323011.7 | hg19 | chr18 | 63,417,488 | 63,548,175 | 130,688 |
ENST00000536984.6 | hg19 | chr18 | 63,417,889 | 63,531,361 | 113,473 |
ENST00000397968.4 | hg19 | chr18 | 63,418,248 | 63,557,573 | 139,326 |
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