RPL18A ribosomal protein L18a
Clinical Significance
MGeND | ClinVar | |
---|---|---|
not provided | 1 | 0 |
Uncertain significance | 0 | 16 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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16 |
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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
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 |
Search Word
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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Search word | : | |
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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 | L18A |
SYNONYM | eL20 |
MIM | 604178 OMIM |
HGNC | HGNC:10311 HGNC |
Ensembl | ENSG00000105640 Ensembl |
AllianceGenome | HGNC:10311 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000222247.10 | hg38 | chr19 | 17,859,910 | 17,863,319 | 3,410 |
ENST00000599870.1 | hg38 | chr19 | 17,860,763 | 17,863,304 | 2,542 |
ENST00000599898.5 | hg38 | chr19 | 17,859,932 | 17,863,315 | 3,384 |
ENST00000600147.5 | hg38 | chr19 | 17,859,921 | 17,864,153 | 4,233 |
ENST00000222247.10 | hg19 | chr19 | 17,970,719 | 17,974,128 | 3,410 |
ENST00000600147.5 | hg19 | chr19 | 17,970,730 | 17,974,962 | 4,233 |
ENST00000599898.5 | hg19 | chr19 | 17,970,741 | 17,974,124 | 3,384 |
ENST00000599870.1 | hg19 | chr19 | 17,971,572 | 17,974,113 | 2,542 |
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