ZNF600 zinc finger protein 600
Information
- Symbol
- ZNF600
- Type
- protein-coding
- Description
- zinc finger protein 600
- Entrez Gene ID
- 162966
- Genome
- hg19
- Position
- chr19:53,267,437-53,290,044
- Genome
- hg38
- Position
- chr19:52,764,184-52,786,791
- HGNC
- HGNC:30951 HGNC
- Ensembl
- ENSG00000189190 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Benign | 0 | 18 |
| Likely benign | 0 | 22 |
| Uncertain significance | 0 | 100 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
140 |
 |
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 | |||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | Entry | Origin | Annotation | |||||||||||
Search Word
| Target data | : |
MGeND data only
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| Filtering | : |
| Name | MGeND | Type | Genome | Size | Chromosome | Start | Stop | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | |||||||||||||||
| Type | ID |
|---|---|
| SYNONYM | KR-ZNF1 |
| HGNC | HGNC:30951 HGNC |
| Ensembl | ENSG00000189190 Ensembl |
| AllianceGenome | HGNC:30951 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000648973.1 | hg38 | chr19 | 52,764,550 | 52,786,807 | 22,258 |
| ENST00000338230.3 | hg38 | chr19 | 52,764,195 | 52,786,763 | 22,569 |
| ENST00000685388.1 | hg38 | chr19 | 52,765,162 | 52,783,482 | 18,321 |
| ENST00000688329.1 | hg38 | chr19 | 52,765,515 | 52,783,440 | 17,926 |
| ENST00000692063.1 | hg38 | chr19 | 52,764,184 | 52,786,791 | 22,608 |
| ENST00000692063.1 | hg19 | chr19 | 53,267,437 | 53,290,044 | 22,608 |
| ENST00000338230.3 | hg19 | chr19 | 53,267,448 | 53,290,016 | 22,569 |
| ENST00000648973.1 | hg19 | chr19 | 53,267,803 | 53,290,060 | 22,258 |
| ENST00000685388.1 | hg19 | chr19 | 53,268,415 | 53,286,735 | 18,321 |
| ENST00000688329.1 | hg19 | chr19 | 53,268,768 | 53,286,693 | 17,926 |
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