MRPL21 mitochondrial ribosomal protein L21
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 4 |
Likely benign | 0 | 4 |
Uncertain significance | 0 | 26 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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34 |
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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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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 | L21mt |
SYNONYM | MRP-L21 |
SYNONYM | bL21m |
MIM | 611834 OMIM |
HGNC | HGNC:14479 HGNC |
Ensembl | ENSG00000197345 Ensembl |
AllianceGenome | HGNC:14479 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000362034.7 | hg38 | chr11 | 68,891,278 | 68,903,832 | 12,555 |
ENST00000450904.6 | hg38 | chr11 | 68,891,276 | 68,903,786 | 12,511 |
ENST00000567045.5 | hg38 | chr11 | 68,892,492 | 68,903,778 | 11,287 |
ENST00000450904.6 | hg19 | chr11 | 68,658,744 | 68,671,254 | 12,511 |
ENST00000362034.7 | hg19 | chr11 | 68,658,746 | 68,671,300 | 12,555 |
ENST00000567045.5 | hg19 | chr11 | 68,659,960 | 68,671,246 | 11,287 |
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