MCPH1-DT MCPH1 divergent transcript
Information
- Symbol
- MCPH1-DT
- Type
- ncRNA
- Description
- MCPH1 divergent transcript
- Entrez Gene ID
- 100287015
- Genome
- hg19
- Position
- chr8:6,261,072-6,264,093
- Genome
- hg38
- Position
- chr8:6,403,551-6,406,572
- HGNC
- HGNC:55599 HGNC
- Ensembl
- ENSG00000246089 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
not provided | 2 | 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 | : | |
Filtering | : |
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 |
---|---|---|---|---|---|
ENST00000500118.4 | hg38 | chr8 | 6,403,551 | 6,406,572 | 3,022 |
ENST00000523225.1 | hg38 | chr8 | 6,405,597 | 6,407,142 | 1,546 |
ENST00000500118.4 | hg19 | chr8 | 6,261,072 | 6,264,093 | 3,022 |
ENST00000523225.1 | hg19 | chr8 | 6,263,118 | 6,264,663 | 1,546 |
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