MRPL35 mitochondrial ribosomal protein L35
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 2 |
Uncertain significance | 0 | 18 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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20 |
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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 |
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 | : | |
Filtering | : |
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 | L35mt |
SYNONYM | MRP-L35 |
SYNONYM | bL35m |
MIM | 611841 OMIM |
HGNC | HGNC:14489 HGNC |
Ensembl | ENSG00000132313 Ensembl |
AllianceGenome | HGNC:14489 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000337109.9 | hg38 | chr2 | 86,199,457 | 86,213,790 | 14,334 |
ENST00000254644.12 | hg38 | chr2 | 86,199,355 | 86,212,838 | 13,484 |
ENST00000409180.1 | hg38 | chr2 | 86,199,463 | 86,213,738 | 14,276 |
ENST00000605125.5 | hg38 | chr2 | 86,199,457 | 86,211,045 | 11,589 |
ENST00000254644.12 | hg19 | chr2 | 86,426,478 | 86,439,961 | 13,484 |
ENST00000605125.5 | hg19 | chr2 | 86,426,580 | 86,438,168 | 11,589 |
ENST00000337109.9 | hg19 | chr2 | 86,426,580 | 86,440,913 | 14,334 |
ENST00000409180.1 | hg19 | chr2 | 86,426,586 | 86,440,861 | 14,276 |
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