CLDN6 claudin 6
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 2 |
Likely benign | 0 | 4 |
Uncertain significance | 0 | 24 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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30 |
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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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Target data | : |
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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 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000396925.1 | hg38 | chr16 | 3,014,712 | 3,020,071 | 5,360 |
ENST00000328796.5 | hg38 | chr16 | 3,014,712 | 3,018,183 | 3,472 |
ENST00000572154.1 | hg38 | chr16 | 3,014,857 | 3,018,170 | 3,314 |
ENST00000328796.5 | hg19 | chr16 | 3,064,713 | 3,068,184 | 3,472 |
ENST00000396925.1 | hg19 | chr16 | 3,064,713 | 3,070,072 | 5,360 |
ENST00000572154.1 | hg19 | chr16 | 3,064,858 | 3,068,171 | 3,314 |
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