PRR20B proline rich 20B
Information
- Symbol
- PRR20B
- Type
- protein-coding
- Description
- proline rich 20B
- Entrez Gene ID
- 729233
- Genome
- hg19
- Position
- chr13:57,721,622-57,724,643
- Genome
- hg38
- Position
- chr13:57,147,488-57,150,509
- HGNC
- HGNC:37220 HGNC
- Ensembl
- ENSG00000204918 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Uncertain significance | 0 | 4 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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4 |
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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 |
Search Word
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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Search word | : | |
Filtering | : |
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 |
---|---|
SYNONYM | PRR20 |
SYNONYM | PRR20A |
SYNONYM | PRR20C |
SYNONYM | PRR20D |
SYNONYM | PRR20E |
HGNC | HGNC:37220 HGNC |
Ensembl | ENSG00000204918 Ensembl |
AllianceGenome | HGNC:37220 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000377930.1 | hg38 | chr13 | 57,147,488 | 57,150,509 | 3,022 |
ENST00000377930.1 | hg19 | chr13 | 57,721,622 | 57,724,643 | 3,022 |
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