CNN2 calponin 2
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Pathogenic | 0 | 4 |
Uncertain significance | 0 | 32 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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32 |
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4 |
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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Target data | : |
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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ENST00000348419.7 | hg38 | chr19 | 1,026,610 | 1,039,068 | 12,459 |
ENST00000568865.3 | hg38 | chr19 | 1,026,631 | 1,038,309 | 11,679 |
ENST00000263097.9 | hg38 | chr19 | 1,026,608 | 1,039,065 | 12,458 |
ENST00000562958.6 | hg38 | chr19 | 1,026,629 | 1,039,068 | 12,440 |
ENST00000565096.6 | hg38 | chr19 | 1,026,618 | 1,039,068 | 12,451 |
ENST00000263097.9 | hg19 | chr19 | 1,026,607 | 1,039,064 | 12,458 |
ENST00000348419.7 | hg19 | chr19 | 1,026,609 | 1,039,067 | 12,459 |
ENST00000565096.6 | hg19 | chr19 | 1,026,617 | 1,039,067 | 12,451 |
ENST00000562958.6 | hg19 | chr19 | 1,026,628 | 1,039,067 | 12,440 |
ENST00000568865.3 | hg19 | chr19 | 1,026,630 | 1,038,308 | 11,679 |
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