DRAP1 DR1 associated protein 1
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 2 |
Uncertain significance | 0 | 20 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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22 |
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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 | : |
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 | NC2-alpha |
MIM | 602289 OMIM |
HGNC | HGNC:3019 HGNC |
Ensembl | ENSG00000175550 Ensembl |
AllianceGenome | HGNC:3019 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000532933.1 | hg38 | chr11 | 65,919,724 | 65,921,554 | 1,831 |
ENST00000312515.7 | hg38 | chr11 | 65,919,426 | 65,921,563 | 2,138 |
ENST00000527119.5 | hg38 | chr11 | 65,919,502 | 65,921,530 | 2,029 |
ENST00000376991.6 | hg38 | chr11 | 65,919,335 | 65,921,448 | 2,114 |
ENST00000376991.6 | hg19 | chr11 | 65,686,806 | 65,688,919 | 2,114 |
ENST00000312515.7 | hg19 | chr11 | 65,686,897 | 65,689,034 | 2,138 |
ENST00000527119.5 | hg19 | chr11 | 65,686,973 | 65,689,001 | 2,029 |
ENST00000532933.1 | hg19 | chr11 | 65,687,195 | 65,689,025 | 1,831 |
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