ARVCF ARVCF delta catenin family member
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 118 |
Likely benign | 0 | 26 |
drug response | 0 | 22 |
not provided | 14 | 0 |
Uncertain significance | 0 | 186 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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14 |
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308 |
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26 |
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
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 |
Search Word
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 |
Search Word
Target data | : |
MGeND data only
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Category | : |
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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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ENST00000406259.1 | hg38 | chr22 | 19,971,228 | 19,990,794 | 19,567 |
ENST00000401994.5 | hg38 | chr22 | 19,971,228 | 19,987,093 | 15,866 |
ENST00000406522.5 | hg38 | chr22 | 19,971,228 | 19,987,093 | 15,866 |
ENST00000263207.8 | hg38 | chr22 | 19,969,896 | 20,016,823 | 46,928 |
ENST00000263207.8 | hg19 | chr22 | 19,957,419 | 20,004,346 | 46,928 |
ENST00000401994.5 | hg19 | chr22 | 19,958,751 | 19,974,616 | 15,866 |
ENST00000406522.5 | hg19 | chr22 | 19,958,751 | 19,974,616 | 15,866 |
ENST00000406259.1 | hg19 | chr22 | 19,958,751 | 19,978,317 | 19,567 |
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