MISP3 MISP family member 3
Information
- Symbol
- MISP3
- Type
- protein-coding
- Description
- MISP family member 3
- Entrez Gene ID
- 113230
- Genome
- hg19
- Position
- chr19:14,183,598-14,185,874
- Genome
- hg38
- Position
- chr19:14,072,786-14,075,062
- HGNC
- HGNC:26963 HGNC
- Ensembl
- ENSG00000141854 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar |
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Ranking
ClinVar | |
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0 |
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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
[No Data.]
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 |
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ENST00000587086.3 | hg38 | chr19 | 14,072,786 | 14,075,062 | 2,277 |
ENST00000269720.6 | hg38 | chr19 | 14,072,536 | 14,075,061 | 2,526 |
ENST00000269720.6 | hg19 | chr19 | 14,183,348 | 14,185,873 | 2,526 |
ENST00000587086.3 | hg19 | chr19 | 14,183,598 | 14,185,874 | 2,277 |
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