ZNF565 zinc finger protein 565
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 6 |
Uncertain significance | 0 | 54 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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60 |
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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 |
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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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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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MIM | 614275 OMIM |
HGNC | HGNC:26726 HGNC |
Ensembl | ENSG00000196357 Ensembl |
AllianceGenome | HGNC:26726 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000355114.9 | hg38 | chr19 | 36,182,294 | 36,246,257 | 63,964 |
ENST00000392173.6 | hg38 | chr19 | 36,182,294 | 36,215,081 | 32,788 |
ENST00000304116.10 | hg38 | chr19 | 36,182,276 | 36,214,665 | 32,390 |
ENST00000304116.10 | hg19 | chr19 | 36,673,178 | 36,705,567 | 32,390 |
ENST00000392173.6 | hg19 | chr19 | 36,673,196 | 36,705,983 | 32,788 |
ENST00000355114.9 | hg19 | chr19 | 36,673,196 | 36,737,159 | 63,964 |
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