ZNF213 zinc finger protein 213
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Benign | 0 | 4 |
| Likely benign | 0 | 4 |
| Uncertain significance | 0 | 64 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
72 |
 |
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
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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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| 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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| 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 | CR53 |
| SYNONYM | ZKSCAN21 |
| SYNONYM | ZSCAN53 |
| MIM | 608387 OMIM |
| HGNC | HGNC:13005 HGNC |
| Ensembl | ENSG00000085644 Ensembl |
| AllianceGenome | HGNC:13005 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000396878.8 | hg38 | chr16 | 3,135,029 | 3,142,804 | 7,776 |
| ENST00000574902.5 | hg38 | chr16 | 3,134,923 | 3,142,803 | 7,881 |
| ENST00000576416.5 | hg38 | chr16 | 3,135,133 | 3,141,779 | 6,647 |
| ENST00000574902.5 | hg19 | chr16 | 3,184,924 | 3,192,804 | 7,881 |
| ENST00000396878.8 | hg19 | chr16 | 3,185,030 | 3,192,805 | 7,776 |
| ENST00000576416.5 | hg19 | chr16 | 3,185,134 | 3,191,780 | 6,647 |
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