ZNF816-ZNF321P ZNF816-ZNF321P readthrough
Information
- Symbol
- ZNF816-ZNF321P
- Type
- protein-coding
- Description
- ZNF816-ZNF321P readthrough
- Entrez Gene ID
- 100529240
- Genome
- hg19
- Position
- chr19:53,431,728-53,466,076
- Genome
- hg38
- Position
- chr19:52,928,475-52,962,823
- HGNC
- HGNC:38879 HGNC
- Ensembl
- ENSG00000221874 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 16 |
Uncertain significance | 0 | 90 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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106 |
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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
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 |
Type | ID |
---|---|
SYNONYM | ZNF816-ZNF321 |
HGNC | HGNC:38879 HGNC |
Ensembl | ENSG00000221874 Ensembl |
AllianceGenome | HGNC:38879 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000391777.3 | hg38 | chr19 | 52,928,475 | 52,962,823 | 34,349 |
ENST00000391777.3 | hg19 | chr19 | 53,431,728 | 53,466,076 | 34,349 |
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