MRPL4 mitochondrial ribosomal protein L4
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 4 |
Uncertain significance | 0 | 8 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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12 |
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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 |
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 |
---|---|
SYNONYM | CGI-28 |
SYNONYM | L4mt |
SYNONYM | uL4m |
MIM | 611823 OMIM |
HGNC | HGNC:14276 HGNC |
Ensembl | ENSG00000105364 Ensembl |
AllianceGenome | HGNC:14276 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000590669.5 | hg38 | chr19 | 10,252,010 | 10,259,125 | 7,116 |
ENST00000588502.5 | hg38 | chr19 | 10,252,276 | 10,258,623 | 6,348 |
ENST00000393733.6 | hg38 | chr19 | 10,252,227 | 10,260,025 | 7,799 |
ENST00000307422.9 | hg38 | chr19 | 10,251,964 | 10,260,043 | 8,080 |
ENST00000253099.11 | hg38 | chr19 | 10,252,214 | 10,260,055 | 7,842 |
ENST00000307422.9 | hg19 | chr19 | 10,362,640 | 10,370,719 | 8,080 |
ENST00000590669.5 | hg19 | chr19 | 10,362,686 | 10,369,801 | 7,116 |
ENST00000253099.11 | hg19 | chr19 | 10,362,890 | 10,370,731 | 7,842 |
ENST00000393733.6 | hg19 | chr19 | 10,362,903 | 10,370,701 | 7,799 |
ENST00000588502.5 | hg19 | chr19 | 10,362,952 | 10,369,299 | 6,348 |
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