RPL38 ribosomal protein L38
Clinical Significance
MGeND | ClinVar |
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Ranking
ClinVar | |
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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 | L38 |
SYNONYM | eL38 |
MIM | 604182 OMIM |
HGNC | HGNC:10349 HGNC |
Ensembl | ENSG00000172809 Ensembl |
AllianceGenome | HGNC:10349 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000534490.5 | hg38 | chr17 | 74,203,694 | 74,209,461 | 5,768 |
ENST00000584577.5 | hg38 | chr17 | 74,203,693 | 74,209,878 | 6,186 |
ENST00000439590.6 | hg38 | chr17 | 74,203,582 | 74,209,880 | 6,299 |
ENST00000533498.1 | hg38 | chr17 | 74,203,704 | 74,209,896 | 6,193 |
ENST00000311111.11 | hg38 | chr17 | 74,203,678 | 74,210,655 | 6,978 |
ENST00000439590.6 | hg19 | chr17 | 72,199,721 | 72,206,019 | 6,299 |
ENST00000311111.11 | hg19 | chr17 | 72,199,817 | 72,206,794 | 6,978 |
ENST00000584577.5 | hg19 | chr17 | 72,199,832 | 72,206,017 | 6,186 |
ENST00000534490.5 | hg19 | chr17 | 72,199,833 | 72,205,600 | 5,768 |
ENST00000533498.1 | hg19 | chr17 | 72,199,843 | 72,206,035 | 6,193 |
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