FARSA phenylalanyl-tRNA synthetase subunit alpha
Information
- Symbol
- FARSA
- Type
- protein-coding
- Description
- phenylalanyl-tRNA synthetase subunit alpha
- Entrez Gene ID
- 2193
- Genome
- hg19
- Position
- chr19:13,033,293-13,044,525
- Genome
- hg38
- Position
- chr19:12,922,479-12,933,711
- MIM
- 602918 OMIM
- HGNC
- HGNC:3592 HGNC
- Ensembl
- ENSG00000179115 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Pathogenic | 0 | 6 |
Likely pathogenic | 0 | 2 |
Benign | 0 | 20 |
Likely benign | 0 | 12 |
Conflicting classifications of pathogenicity | 0 | 2 |
not provided | 1 | 0 |
Uncertain significance | 0 | 54 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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2 |
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88 |
![]() |
2 |
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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Category | : |
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Search word | : | |
Filtering | : |
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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Category | : |
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Search word | : | |
Filtering | : |
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
|
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 | CML33 |
SYNONYM | FARSL |
SYNONYM | FARSLA |
SYNONYM | FRSA |
SYNONYM | PheHA |
SYNONYM | RILDBC2 |
MIM | 602918 OMIM |
HGNC | HGNC:3592 HGNC |
Ensembl | ENSG00000179115 Ensembl |
AllianceGenome | HGNC:3592 |
Descrption | Source | Links |
---|
ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000314606.9 | hg38 | chr19 | 12,922,479 | 12,933,711 | 11,233 |
ENST00000588025.5 | hg38 | chr19 | 12,922,479 | 12,934,037 | 11,559 |
ENST00000423140.6 | hg38 | chr19 | 12,922,480 | 12,933,714 | 11,235 |
ENST00000314606.9 | hg19 | chr19 | 13,033,293 | 13,044,525 | 11,233 |
ENST00000588025.5 | hg19 | chr19 | 13,033,293 | 13,044,851 | 11,559 |
ENST00000423140.6 | hg19 | chr19 | 13,033,294 | 13,044,528 | 11,235 |
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