ZNF527 zinc finger protein 527
Information
- Symbol
- ZNF527
- Type
- protein-coding
- Description
- zinc finger protein 527
- Entrez Gene ID
- 84503
- Genome
- hg19
- Position
- chr19:37,862,001-37,883,968
- Genome
- hg38
- Position
- chr19:37,371,099-37,393,066
- HGNC
- HGNC:29385 HGNC
- Ensembl
- ENSG00000189164 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 4 |
Likely benign | 0 | 2 |
Uncertain significance | 0 | 38 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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44 |
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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 |
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Entry | Origin | Type | Annotation | Entry | Origin | Annotation |
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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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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 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000483919.5 | hg38 | chr19 | 37,371,159 | 37,385,644 | 14,486 |
ENST00000587349.1 | hg38 | chr19 | 37,371,194 | 37,392,894 | 21,701 |
ENST00000436120.7 | hg38 | chr19 | 37,371,099 | 37,393,066 | 21,968 |
ENST00000436120.7 | hg19 | chr19 | 37,862,001 | 37,883,968 | 21,968 |
ENST00000483919.5 | hg19 | chr19 | 37,862,061 | 37,876,546 | 14,486 |
ENST00000587349.1 | hg19 | chr19 | 37,862,096 | 37,883,796 | 21,701 |
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