FARSB phenylalanyl-tRNA synthetase subunit beta

Information
Symbol
FARSB
Type
protein-coding
Description
phenylalanyl-tRNA synthetase subunit beta
Entrez Gene ID
10056
Genome
hg19
Position
chr2:223,431,618-223,520,811
Genome
hg38
Position
chr2:222,566,899-222,656,092
MIM
609690 OMIM
HGNC
HGNC:17800 HGNC
Ensembl
ENSG00000116120 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 0 22
Likely pathogenic 0 8
Benign 0 30
Likely benign 0 112
Conflicting classifications of pathogenicity 0 4
Uncertain significance 0 152
Ranking
ClinVar
0
0
52
256
4
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
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
Category :
Search word :
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
TypeID
SYNONYM FARSLB
SYNONYM FRSB
SYNONYM HSPC173
SYNONYM NEDBLLA
SYNONYM PheHB
SYNONYM PheRS
SYNONYM RILDBC
SYNONYM RILDBC1
SYNONYM RJBS
MIM 609690 OMIM
HGNC HGNC:17800 HGNC
Ensembl ENSG00000116120 Ensembl
AllianceGenome HGNC:17800
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000281828.8 hg38 chr2 222,566,899 222,656,092 89,194
ENST00000281828.8 hg19 chr2 223,431,618 223,520,811 89,194
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