DEPDC7 DEP domain containing 7
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 2 |
not provided | 1 | 0 |
Uncertain significance | 0 | 26 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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28 |
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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
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 |
Search Word
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 | TR2 |
SYNONYM | dJ85M6.4 |
MIM | 612294 OMIM |
HGNC | HGNC:29899 HGNC |
Ensembl | ENSG00000121690 Ensembl |
AllianceGenome | HGNC:29899 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000311388.7 | hg38 | chr11 | 33,016,164 | 33,033,582 | 17,419 |
ENST00000241051.8 | hg38 | chr11 | 33,015,878 | 33,033,582 | 17,705 |
ENST00000241051.8 | hg19 | chr11 | 33,037,424 | 33,055,128 | 17,705 |
ENST00000311388.7 | hg19 | chr11 | 33,037,710 | 33,055,128 | 17,419 |
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