ZNF75A zinc finger protein 75A
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Likely benign | 0 | 6 |
| Uncertain significance | 0 | 22 |
Ranking
| ClinVar | |
|---|---|
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0 |
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0 |
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0 |
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28 |
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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 | |||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 |
|---|---|
| MIM | 601473 OMIM |
| HGNC | HGNC:13146 HGNC |
| Ensembl | ENSG00000162086 Ensembl |
| AllianceGenome | HGNC:13146 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000617839.1 | hg38 | chr16 | 3,311,790 | 3,317,925 | 6,136 |
| ENST00000612186.1 | hg38 | chr16 | 3,308,332 | 3,309,449 | 1,118 |
| ENST00000574298.6 | hg38 | chr16 | 3,305,472 | 3,318,852 | 13,381 |
| ENST00000669516.2 | hg38 | chr16 | 3,305,497 | 3,318,851 | 13,355 |
| ENST00000574298.6 | hg19 | chr16 | 3,355,472 | 3,368,852 | 13,381 |
| ENST00000669516.2 | hg19 | chr16 | 3,355,497 | 3,368,851 | 13,355 |
| ENST00000612186.1 | hg19 | chr16 | 3,358,332 | 3,359,449 | 1,118 |
| ENST00000617839.1 | hg19 | chr16 | 3,361,790 | 3,367,925 | 6,136 |
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