RNF151 ring finger protein 151
Information
- Symbol
- RNF151
- Type
- protein-coding
- Description
- ring finger protein 151
- Entrez Gene ID
- 146310
- Genome
- hg19
- Position
- chr16:2,016,857-2,018,950
- Genome
- hg38
- Position
- chr16:1,966,856-1,968,949
- HGNC
- HGNC:23235 HGNC
- Ensembl
- ENSG00000179580 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 8 |
Uncertain significance | 0 | 44 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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52 |
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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 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000569714.6 | hg38 | chr16 | 1,966,856 | 1,968,949 | 2,094 |
ENST00000321392.4 | hg38 | chr16 | 1,967,273 | 1,968,975 | 1,703 |
ENST00000569210.6 | hg38 | chr16 | 1,966,823 | 1,968,948 | 2,126 |
ENST00000569210.6 | hg19 | chr16 | 2,016,824 | 2,018,949 | 2,126 |
ENST00000569714.6 | hg19 | chr16 | 2,016,857 | 2,018,950 | 2,094 |
ENST00000321392.4 | hg19 | chr16 | 2,017,274 | 2,018,976 | 1,703 |
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