NOP58 NOP58 ribonucleoprotein
Clinical Significance
MGeND | ClinVar | |
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Uncertain significance | 0 | 30 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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30 |
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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
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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 |
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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 | HSPC120 |
SYNONYM | NOP5 |
SYNONYM | NOP5/NOP58 |
MIM | 616742 OMIM |
HGNC | HGNC:29926 HGNC |
Ensembl | ENSG00000055044 Ensembl |
AllianceGenome | HGNC:29926 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000264279.10 | hg38 | chr2 | 202,265,763 | 202,303,661 | 37,899 |
ENST00000264279.10 | hg19 | chr2 | 203,130,486 | 203,168,384 | 37,899 |
Key | Value |
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strand | + |
start | 203,130,438 |
Gene Symbol | NOP58 |
Entrez GeneId | 51,602 |
Chr Band | 2q33.1 |
end | 203,168,383 |
chr | chr2 |
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