FSTL3 follistatin like 3
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 2 |
Uncertain significance | 0 | 44 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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46 |
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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
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Target data | : |
MGeND data only
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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 |
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MGeND data only
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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 |
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MGeND data only
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Name | MGeND | Type | Genome | Gene symbol | Chromosome | Genomic start | Genomic stop | Strand | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
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Entry | Origin | Type | Annotation |
Type | ID |
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SYNONYM | FLRG |
SYNONYM | FSRP |
MIM | 605343 OMIM |
HGNC | HGNC:3973 HGNC |
Ensembl | ENSG00000070404 Ensembl |
AllianceGenome | HGNC:3973 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000588773.5 | hg38 | chr19 | 680,715 | 682,107 | 1,393 |
ENST00000592947.5 | hg38 | chr19 | 680,707 | 683,392 | 2,686 |
ENST00000605925.3 | hg38 | chr19 | 680,751 | 682,107 | 1,357 |
ENST00000166139.9 | hg38 | chr19 | 676,392 | 683,385 | 6,994 |
ENST00000166139.9 | hg19 | chr19 | 676,392 | 683,385 | 6,994 |
ENST00000592947.5 | hg19 | chr19 | 680,707 | 683,392 | 2,686 |
ENST00000588773.5 | hg19 | chr19 | 680,715 | 682,107 | 1,393 |
ENST00000605925.3 | hg19 | chr19 | 680,751 | 682,107 | 1,357 |
Key | Value |
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strand | + |
UniProt | OG |
start | 676,388 |
Gene Symbol | FSTL3 |
Entrez GeneId | 10,272 |
Chr Band | 19p13 |
end | 683,391 |
chr | chr19 |
Name | follistatin-like 3 (secreted glycoprotein) |
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