POP7 POP7 homolog, ribonuclease P/MRP subunit
Information
- Symbol
- POP7
- Type
- protein-coding
- Description
- POP7 homolog, ribonuclease P/MRP subunit
- Entrez Gene ID
- 10248
- Genome
- hg19
- Position
- chr7:100,303,744-100,305,109
- Genome
- hg38
- Position
- chr7:100,706,121-100,707,486
- MIM
- 606113 OMIM
- HGNC
- HGNC:19949 HGNC
- Ensembl
- ENSG00000172336 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Uncertain significance | 0 | 22 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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22 |
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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 |
Type | ID |
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SYNONYM | 0610037N12Rik |
SYNONYM | RPP2 |
SYNONYM | RPP20 |
MIM | 606113 OMIM |
HGNC | HGNC:19949 HGNC |
Ensembl | ENSG00000172336 Ensembl |
AllianceGenome | HGNC:19949 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000303151.5 | hg38 | chr7 | 100,706,121 | 100,707,486 | 1,366 |
ENST00000303151.5 | hg19 | chr7 | 100,303,744 | 100,305,109 | 1,366 |
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