POP4 POP4 homolog, ribonuclease P/MRP subunit
Information
- Symbol
- POP4
- Type
- protein-coding
- Description
- POP4 homolog, ribonuclease P/MRP subunit
- Entrez Gene ID
- 10775
- Genome
- hg19
- Position
- chr19:30,097,190-30,108,144
- Genome
- hg38
- Position
- chr19:29,606,283-29,617,237
- MIM
- 606114 OMIM
- HGNC
- HGNC:30081 HGNC
- Ensembl
- ENSG00000105171 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 6 |
Uncertain significance | 0 | 20 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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26 |
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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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Category | : |
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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 | RPP29 |
MIM | 606114 OMIM |
HGNC | HGNC:30081 HGNC |
Ensembl | ENSG00000105171 Ensembl |
AllianceGenome | HGNC:30081 |
Descrption | Source | Links |
---|
ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000585603.6 | hg38 | chr19 | 29,606,283 | 29,617,237 | 10,955 |
ENST00000221770.7 | hg38 | chr19 | 29,606,294 | 29,617,237 | 10,944 |
ENST00000585603.6 | hg19 | chr19 | 30,097,190 | 30,108,144 | 10,955 |
ENST00000221770.7 | hg19 | chr19 | 30,097,201 | 30,108,144 | 10,944 |
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