RNF222 ring finger protein 222
Information
- Symbol
- RNF222
- Type
- protein-coding
- Description
- ring finger protein 222
- Entrez Gene ID
- 643904
- Genome
- hg19
- Position
- chr17:8,294,020-8,301,145
- Genome
- hg38
- Position
- chr17:8,390,702-8,397,827
- HGNC
- HGNC:34517 HGNC
- Ensembl
- ENSG00000189051 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 2 |
Uncertain significance | 0 | 42 |
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 |
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ENST00000344001.3 | hg38 | chr17 | 8,390,704 | 8,393,489 | 2,786 |
ENST00000399398.3 | hg38 | chr17 | 8,390,702 | 8,397,827 | 7,126 |
ENST00000399398.3 | hg19 | chr17 | 8,294,020 | 8,301,145 | 7,126 |
ENST00000344001.3 | hg19 | chr17 | 8,294,022 | 8,296,807 | 2,786 |
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