SARS2 seryl-tRNA synthetase 2, mitochondrial
Information
- Symbol
- SARS2
- Type
- protein-coding
- Description
- seryl-tRNA synthetase 2, mitochondrial
- Entrez Gene ID
- 54938
- Genome
- hg19
- Position
- chr19:39,406,204-39,421,401
- Genome
- hg38
- Position
- chr19:38,915,564-38,930,761
- MIM
- 612804 OMIM
- HGNC
- HGNC:17697 HGNC
- Ensembl
- ENSG00000104835 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Pathogenic | 0 | 8 |
| Likely pathogenic | 0 | 6 |
| Benign | 0 | 78 |
| Likely benign | 0 | 204 |
| Conflicting classifications of pathogenicity | 0 | 44 |
| Uncertain significance | 0 | 216 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
102 |
 |
380 |
 |
12 |
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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| Category | : |
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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
|
| Category | : |
|
| Search word | : | |
| 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 | SARS |
| SYNONYM | SARSM |
| SYNONYM | SERS |
| SYNONYM | SYS |
| SYNONYM | SerRS |
| SYNONYM | SerRSmt |
| SYNONYM | mtSerRS |
| MIM | 612804 OMIM |
| HGNC | HGNC:17697 HGNC |
| Ensembl | ENSG00000104835 Ensembl |
| AllianceGenome | HGNC:17697 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000600042.5 | hg38 | chr19 | 38,915,564 | 38,930,761 | 15,198 |
| ENST00000430193.7 | hg38 | chr19 | 38,915,299 | 38,930,758 | 15,460 |
| ENST00000594171.5 | hg38 | chr19 | 38,915,269 | 38,930,133 | 14,865 |
| ENST00000221431.11 | hg38 | chr19 | 38,915,266 | 38,930,763 | 15,498 |
| ENST00000598831.5 | hg38 | chr19 | 38,915,318 | 38,917,827 | 2,510 |
| ENST00000221431.11 | hg19 | chr19 | 39,405,906 | 39,421,403 | 15,498 |
| ENST00000594171.5 | hg19 | chr19 | 39,405,909 | 39,420,773 | 14,865 |
| ENST00000430193.7 | hg19 | chr19 | 39,405,939 | 39,421,398 | 15,460 |
| ENST00000598831.5 | hg19 | chr19 | 39,405,958 | 39,408,467 | 2,510 |
| ENST00000600042.5 | hg19 | chr19 | 39,406,204 | 39,421,401 | 15,198 |
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