ZNF701 zinc finger protein 701
Information
- Symbol
- ZNF701
- Type
- protein-coding
- Description
- zinc finger protein 701
- Entrez Gene ID
- 55762
- Genome
- hg19
- Position
- chr19:53,073,554-53,087,689
- Genome
- hg38
- Position
- chr19:52,570,301-52,584,436
- HGNC
- HGNC:25597 HGNC
- Ensembl
- ENSG00000167562 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 12 |
Uncertain significance | 0 | 74 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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86 |
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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 |
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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 |
Search Word
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 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000301093.6 | hg38 | chr19 | 52,570,301 | 52,584,436 | 14,136 |
ENST00000540331.1 | hg38 | chr19 | 52,570,664 | 52,587,174 | 16,511 |
ENST00000391785.8 | hg38 | chr19 | 52,570,287 | 52,587,174 | 16,888 |
ENST00000391785.8 | hg19 | chr19 | 53,073,540 | 53,090,427 | 16,888 |
ENST00000301093.6 | hg19 | chr19 | 53,073,554 | 53,087,689 | 14,136 |
ENST00000540331.1 | hg19 | chr19 | 53,073,917 | 53,090,427 | 16,511 |
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