FGF11 fibroblast growth factor 11
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 4 |
Uncertain significance | 0 | 22 |
Ranking
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0 |
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0 |
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26 |
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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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Variant name | Gene | AA change | CDS | Japanese frequency |
TogoVar | MGeND | Genome | ClinVar | CIViC evidence | DisGeNET entry | COSMIC occurrence |
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Entry | Origin | Type | Annotation | Entry | Origin | Annotation |
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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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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 | FGF-11 |
SYNONYM | FHF-3 |
SYNONYM | FHF3 |
MIM | 601514 OMIM |
HGNC | HGNC:3667 HGNC |
Ensembl | ENSG00000161958 Ensembl |
AllianceGenome | HGNC:3667 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000575398.5 | hg38 | chr17 | 7,440,742 | 7,443,556 | 2,815 |
ENST00000575082.5 | hg38 | chr17 | 7,440,743 | 7,444,902 | 4,160 |
ENST00000572907.5 | hg38 | chr17 | 7,439,880 | 7,443,428 | 3,549 |
ENST00000293829.9 | hg38 | chr17 | 7,439,512 | 7,444,937 | 5,426 |
ENST00000575235.5 | hg38 | chr17 | 7,438,273 | 7,443,331 | 5,059 |
ENST00000575235.5 | hg19 | chr17 | 7,341,592 | 7,346,650 | 5,059 |
ENST00000293829.9 | hg19 | chr17 | 7,342,831 | 7,348,256 | 5,426 |
ENST00000572907.5 | hg19 | chr17 | 7,343,199 | 7,346,747 | 3,549 |
ENST00000575398.5 | hg19 | chr17 | 7,344,061 | 7,346,875 | 2,815 |
ENST00000575082.5 | hg19 | chr17 | 7,344,062 | 7,348,221 | 4,160 |
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