MRPL19 mitochondrial ribosomal protein L19
Information
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Benign | 0 | 2 |
| Likely benign | 0 | 10 |
| Uncertain significance | 0 | 66 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
78 |
 |
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 | |||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | Entry | Origin | Annotation | |||||||||||
Search Word
| Target data | : |
MGeND data only
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| Filtering | : |
| Name | MGeND | Type | Genome | Size | Chromosome | Start | Stop | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | ||||||||||||||
Search Word
| Target data | : |
MGeND data only
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| Category | : |
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| Filtering | : |
| Name | MGeND | Type | Genome | Gene symbol | Chromosome | Genomic start | Genomic stop | Strand | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | |||||||||||||||
| Type | ID |
|---|---|
| SYNONYM | L15mt |
| SYNONYM | L19mt |
| SYNONYM | MRP-L15 |
| SYNONYM | MRP-L19 |
| SYNONYM | MRPL15 |
| SYNONYM | RLX1 |
| SYNONYM | RPML15 |
| SYNONYM | bL19m |
| MIM | 611832 OMIM |
| HGNC | HGNC:14052 HGNC |
| Ensembl | ENSG00000115364 Ensembl |
| AllianceGenome | HGNC:14052 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000393909.7 | hg38 | chr2 | 75,646,783 | 75,662,206 | 15,424 |
| ENST00000409374.5 | hg38 | chr2 | 75,646,803 | 75,670,753 | 23,951 |
| ENST00000358788.10 | hg38 | chr2 | 75,646,794 | 75,690,759 | 43,966 |
| ENST00000393909.7 | hg19 | chr2 | 75,873,909 | 75,889,332 | 15,424 |
| ENST00000358788.10 | hg19 | chr2 | 75,873,920 | 75,917,885 | 43,966 |
| ENST00000409374.5 | hg19 | chr2 | 75,873,929 | 75,897,879 | 23,951 |
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