ZCWPW1 zinc finger CW-type and PWWP domain containing 1
Information
- Symbol
- ZCWPW1
- Type
- protein-coding
- Description
- zinc finger CW-type and PWWP domain containing 1
- Entrez Gene ID
- 55063
- Genome
- hg19
- Position
- chr7:99,998,495-100,026,326
- Genome
- hg38
- Position
- chr7:100,400,872-100,428,703
- MIM
- 618900 OMIM
- HGNC
- HGNC:23486 HGNC
- Ensembl
- ENSG00000078487 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 11 | 0 |
Likely benign | 0 | 8 |
not provided | 1 | 0 |
Uncertain significance | 0 | 56 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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64 |
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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
Locus Zoom
Variants
Search Word
Target data | : |
MGeND data only
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Category | : |
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Search word | : | |
Filtering | : |
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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Category | : |
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Search word | : | |
Filtering | : |
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
|
Category | : |
|
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 | ZCW1 |
MIM | 618900 OMIM |
HGNC | HGNC:23486 HGNC |
Ensembl | ENSG00000078487 Ensembl |
AllianceGenome | HGNC:23486 |
Descrption | Source | Links |
---|
ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000490721.5 | hg38 | chr7 | 100,400,855 | 100,419,877 | 19,023 |
ENST00000684423.1 | hg38 | chr7 | 100,400,872 | 100,428,703 | 27,832 |
ENST00000360951.8 | hg38 | chr7 | 100,400,873 | 100,428,664 | 27,792 |
ENST00000398027.6 | hg38 | chr7 | 100,400,853 | 100,428,679 | 27,827 |
ENST00000398027.6 | hg19 | chr7 | 99,998,476 | 100,026,302 | 27,827 |
ENST00000490721.5 | hg19 | chr7 | 99,998,478 | 100,017,500 | 19,023 |
ENST00000684423.1 | hg19 | chr7 | 99,998,495 | 100,026,326 | 27,832 |
ENST00000360951.8 | hg19 | chr7 | 99,998,496 | 100,026,287 | 27,792 |
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