RPP21 ribonuclease P/MRP subunit p21
Information
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Uncertain significance | 0 | 2 |
Ranking
| ClinVar | |
|---|---|
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0 |
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0 |
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0 |
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2 |
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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 | |||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | Entry | Origin | Annotation | |||||||||||
Search Word
| Target data | : |
MGeND data only
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| Filtering | : |
| Name | MGeND | Type | Genome | Size | Chromosome | Start | Stop | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | |||||||||||||||
| Type | ID |
|---|---|
| SYNONYM | C6orf135 |
| SYNONYM | CAT60 |
| MIM | 612524 OMIM |
| HGNC | HGNC:21300 HGNC |
| Ensembl | ENSG00000241370 Ensembl |
| AllianceGenome | HGNC:21300 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000428040.6 | hg38 | chr6 | 30,345,159 | 30,346,857 | 1,699 |
| ENST00000433076.6 | hg38 | chr6 | 30,345,131 | 30,346,857 | 1,727 |
| ENST00000442966.7 | hg38 | chr6 | 30,345,156 | 30,346,857 | 1,702 |
| ENST00000436442.2 | hg38 | chr6 | 30,345,169 | 30,346,857 | 1,689 |
| ENST00000433076.6 | hg19 | chr6 | 30,312,908 | 30,314,634 | 1,727 |
| ENST00000442966.7 | hg19 | chr6 | 30,312,933 | 30,314,634 | 1,702 |
| ENST00000428040.6 | hg19 | chr6 | 30,312,936 | 30,314,634 | 1,699 |
| ENST00000436442.2 | hg19 | chr6 | 30,312,946 | 30,314,634 | 1,689 |
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