DIAPH2-AS1 DIAPH2 antisense RNA 1
Clinical Significance
MGeND | ClinVar | |
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not provided | 6 | 0 |
Ranking
ClinVar | |
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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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Search word | : | |
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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 | EPAG |
MIM | 300347 OMIM |
HGNC | HGNC:16972 HGNC |
Ensembl | ENSG00000236256 Ensembl |
AllianceGenome | HGNC:16972 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000439759.6 | hg38 | chrX | 97,431,286 | 97,564,505 | 133,220 |
ENST00000542084.1 | hg38 | chrX | 97,602,830 | 97,642,589 | 39,760 |
ENST00000579945.1 | hg38 | chrX | 97,528,365 | 97,564,533 | 36,169 |
ENST00000445414.1 | hg38 | chrX | 97,533,173 | 97,617,259 | 84,087 |
ENST00000439759.6 | hg19 | chrX | 96,686,285 | 96,819,504 | 133,220 |
ENST00000579945.1 | hg19 | chrX | 96,783,364 | 96,819,532 | 36,169 |
ENST00000445414.1 | hg19 | chrX | 96,788,172 | 96,872,258 | 84,087 |
ENST00000542084.1 | hg19 | chrX | 96,857,829 | 96,897,588 | 39,760 |
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