ZNF699 zinc finger protein 699
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Pathogenic | 0 | 12 |
Likely benign | 0 | 6 |
Uncertain significance | 0 | 62 |
Ranking
ClinVar | |
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0 |
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0 |
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4 |
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68 |
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8 |
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
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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 |
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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 |
Type | ID |
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SYNONYM | DEGCAGS |
SYNONYM | hang |
MIM | 609571 OMIM |
HGNC | HGNC:24750 HGNC |
Ensembl | ENSG00000196110 Ensembl |
AllianceGenome | HGNC:24750 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000308650.4 | hg38 | chr19 | 9,295,310 | 9,305,119 | 9,810 |
ENST00000591998.6 | hg38 | chr19 | 9,291,140 | 9,309,838 | 18,699 |
ENST00000591998.6 | hg19 | chr19 | 9,401,816 | 9,420,514 | 18,699 |
ENST00000308650.4 | hg19 | chr19 | 9,405,986 | 9,415,795 | 9,810 |
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