RPL21 ribosomal protein L21
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Pathogenic | 0 | 2 |
Benign | 0 | 18 |
Likely benign | 0 | 10 |
Uncertain significance | 0 | 14 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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4 |
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38 |
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2 |
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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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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HGNC | HGNC:10313 HGNC |
SYNONYM | HYPT12 |
SYNONYM | L21 |
SYNONYM | eL21 |
MIM | 603636 OMIM |
Ensembl | ENSG00000122026 Ensembl |
AllianceGenome | HGNC:10313 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000311549.11 | hg38 | chr13 | 27,251,558 | 27,256,568 | 5,011 |
ENST00000326092.8 | hg38 | chr13 | 27,251,597 | 27,256,568 | 4,972 |
ENST00000319826.8 | hg38 | chr13 | 27,251,583 | 27,256,568 | 4,986 |
ENST00000272274.8 | hg38 | chr13 | 27,251,579 | 27,256,568 | 4,990 |
ENST00000311549.11 | hg19 | chr13 | 27,825,695 | 27,830,705 | 5,011 |
ENST00000272274.8 | hg19 | chr13 | 27,825,716 | 27,830,705 | 4,990 |
ENST00000319826.8 | hg19 | chr13 | 27,825,720 | 27,830,705 | 4,986 |
ENST00000326092.8 | hg19 | chr13 | 27,825,734 | 27,830,705 | 4,972 |
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