RPL28 ribosomal protein L28
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 8 |
Likely benign | 0 | 6 |
Uncertain significance | 0 | 32 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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2 |
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44 |
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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 |
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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 | L28 |
SYNONYM | eL28 |
MIM | 603638 OMIM |
HGNC | HGNC:10330 HGNC |
Ensembl | ENSG00000108107 Ensembl |
AllianceGenome | HGNC:10330 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000558752.1 | hg38 | chr19 | 55,386,357 | 55,387,231 | 875 |
ENST00000431533.6 | hg38 | chr19 | 55,385,932 | 55,387,036 | 1,105 |
ENST00000559463.5 | hg38 | chr19 | 55,385,961 | 55,388,373 | 2,413 |
ENST00000558815.5 | hg38 | chr19 | 55,385,932 | 55,391,803 | 5,872 |
ENST00000560583.5 | hg38 | chr19 | 55,385,934 | 55,388,888 | 2,955 |
ENST00000560055.5 | hg38 | chr19 | 55,385,936 | 55,403,250 | 17,315 |
ENST00000344063.7 | hg38 | chr19 | 55,385,932 | 55,392,085 | 6,154 |
ENST00000428193.6 | hg38 | chr19 | 55,385,932 | 55,387,610 | 1,679 |
ENST00000558131.1 | hg38 | chr19 | 55,386,350 | 55,388,373 | 2,024 |
ENST00000431533.6 | hg19 | chr19 | 55,897,300 | 55,898,404 | 1,105 |
ENST00000428193.6 | hg19 | chr19 | 55,897,300 | 55,898,978 | 1,679 |
ENST00000558815.5 | hg19 | chr19 | 55,897,300 | 55,903,171 | 5,872 |
ENST00000344063.7 | hg19 | chr19 | 55,897,300 | 55,903,453 | 6,154 |
ENST00000560583.5 | hg19 | chr19 | 55,897,302 | 55,900,256 | 2,955 |
ENST00000560055.5 | hg19 | chr19 | 55,897,304 | 55,914,618 | 17,315 |
ENST00000559463.5 | hg19 | chr19 | 55,897,329 | 55,899,741 | 2,413 |
ENST00000558131.1 | hg19 | chr19 | 55,897,718 | 55,899,741 | 2,024 |
ENST00000558752.1 | hg19 | chr19 | 55,897,725 | 55,898,599 | 875 |
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