ZNF780A zinc finger protein 780A
Information
- Symbol
- ZNF780A
- Type
- protein-coding
- Description
- zinc finger protein 780A
- Entrez Gene ID
- 284323
- Genome
- hg19
- Position
- chr19:40,580,423-40,596,142
- Genome
- hg38
- Position
- chr19:40,074,516-40,090,235
- HGNC
- HGNC:27603 HGNC
- Ensembl
- ENSG00000197782 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 6 |
Uncertain significance | 0 | 92 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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98 |
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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 | ZNF780 |
HGNC | HGNC:27603 HGNC |
Ensembl | ENSG00000197782 Ensembl |
AllianceGenome | HGNC:27603 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000683561.1 | hg38 | chr19 | 40,073,045 | 40,090,943 | 17,899 |
ENST00000594395.5 | hg38 | chr19 | 40,074,516 | 40,090,235 | 15,720 |
ENST00000450241.6 | hg38 | chr19 | 40,069,152 | 40,090,888 | 21,737 |
ENST00000595687.6 | hg38 | chr19 | 40,073,180 | 40,090,888 | 17,709 |
ENST00000340963.9 | hg38 | chr19 | 40,072,993 | 40,090,903 | 17,911 |
ENST00000414720.6 | hg38 | chr19 | 40,071,006 | 40,090,938 | 19,933 |
ENST00000455521.5 | hg38 | chr19 | 40,072,993 | 40,090,938 | 17,946 |
ENST00000450241.6 | hg19 | chr19 | 40,575,059 | 40,596,795 | 21,737 |
ENST00000414720.6 | hg19 | chr19 | 40,576,913 | 40,596,845 | 19,933 |
ENST00000340963.9 | hg19 | chr19 | 40,578,900 | 40,596,810 | 17,911 |
ENST00000455521.5 | hg19 | chr19 | 40,578,900 | 40,596,845 | 17,946 |
ENST00000683561.1 | hg19 | chr19 | 40,578,952 | 40,596,850 | 17,899 |
ENST00000595687.6 | hg19 | chr19 | 40,579,087 | 40,596,795 | 17,709 |
ENST00000594395.5 | hg19 | chr19 | 40,580,423 | 40,596,142 | 15,720 |
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