RPS16 ribosomal protein S16
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 2 |
Uncertain significance | 0 | 10 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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12 |
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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 |
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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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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 | S16 |
SYNONYM | uS9 |
MIM | 603675 OMIM |
HGNC | HGNC:10396 HGNC |
Ensembl | ENSG00000105193 Ensembl |
AllianceGenome | HGNC:10396 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000599539.5 | hg38 | chr19 | 39,433,207 | 39,435,915 | 2,709 |
ENST00000339471.8 | hg38 | chr19 | 39,433,207 | 39,435,936 | 2,730 |
ENST00000251453.8 | hg38 | chr19 | 39,433,137 | 39,435,949 | 2,813 |
ENST00000601655.5 | hg38 | chr19 | 39,433,217 | 39,435,941 | 2,725 |
ENST00000251453.8 | hg19 | chr19 | 39,923,777 | 39,926,589 | 2,813 |
ENST00000599539.5 | hg19 | chr19 | 39,923,847 | 39,926,555 | 2,709 |
ENST00000339471.8 | hg19 | chr19 | 39,923,847 | 39,926,576 | 2,730 |
ENST00000601655.5 | hg19 | chr19 | 39,923,857 | 39,926,581 | 2,725 |
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