FASLG Fas ligand

Information
Symbol
FASLG
Type
protein-coding
Description
Fas ligand
Entrez Gene ID
356
Genome
hg19
Position
chr1:172,628,243-172,636,016
Genome
hg38
Position
chr1:172,659,103-172,666,876
MIM
134638 OMIM
HGNC
HGNC:11936 HGNC
Ensembl
ENSG00000117560 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 0 6
Benign 0 36
Likely benign 0 132
Conflicting classifications of pathogenicity 0 14
not provided 0 8
Uncertain significance 0 172
Ranking
ClinVar
0
0
36
298
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
[No Data.]
Locus Zoom
Variants
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
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 ALPS1B
SYNONYM APT1LG1
SYNONYM APTL
SYNONYM CD178
SYNONYM CD95-L
SYNONYM CD95L
SYNONYM FASL
SYNONYM TNFSF6
SYNONYM TNLG1A
MIM 134638 OMIM
HGNC HGNC:11936 HGNC
Ensembl ENSG00000117560 Ensembl
AllianceGenome HGNC:11936
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000340030.4 hg38 chr1 172,659,144 172,666,075 6,932
ENST00000367721.3 hg38 chr1 172,659,103 172,666,876 7,774
ENST00000367721.3 hg19 chr1 172,628,243 172,636,016 7,774
ENST00000340030.4 hg19 chr1 172,628,284 172,635,215 6,932
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