FST follistatin

Information
Symbol
FST
Type
protein-coding
Description
follistatin
Entrez Gene ID
10468
Genome
hg19
Position
chr5:52,776,459-52,782,964
Genome
hg38
Position
chr5:53,480,629-53,487,134
MIM
136470 OMIM
HGNC
HGNC:3971 HGNC
Ensembl
ENSG00000134363 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 8
Likely benign 0 2
Conflicting classifications of pathogenicity 0 2
Uncertain significance 0 12
Ranking
ClinVar
0
0
0
22
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 FS
MIM 136470 OMIM
HGNC HGNC:3971 HGNC
Ensembl ENSG00000134363 Ensembl
AllianceGenome HGNC:3971
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000396947.7 hg38 chr5 53,480,626 53,487,106 6,481
ENST00000256759.8 hg38 chr5 53,480,629 53,487,134 6,506
ENST00000396947.7 hg19 chr5 52,776,456 52,782,936 6,481
ENST00000256759.8 hg19 chr5 52,776,459 52,782,964 6,506
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