FOXL3 forkhead box L3

Information
Symbol
FOXL3
Type
protein-coding
Description
forkhead box L3
Entrez Gene ID
116033993
Genome
hg19
Position
chr7:330,136-331,454
Genome
hg38
Position
chr7:290,170-291,488
HGNC
HGNC:54201 HGNC
Ensembl
ENSG00000248767 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Uncertain significance 0 8
Ranking
ClinVar
0
0
0
8
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
Category :
Search word :
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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
HGNC HGNC:54201 HGNC
Ensembl ENSG00000248767 Ensembl
AllianceGenome HGNC:54201
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000506382.2 hg38 chr7 290,170 291,488 1,319
ENST00000506382.2 hg19 chr7 330,136 331,454 1,319
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