FGF17 fibroblast growth factor 17
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Pathogenic | 0 | 4 |
Benign | 0 | 24 |
Likely benign | 0 | 38 |
risk factor | 0 | 2 |
Uncertain significance | 0 | 26 |
Ranking
ClinVar | |
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0 |
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0 |
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4 |
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82 |
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6 |
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
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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-13 |
SYNONYM | FGF-17 |
SYNONYM | HH20 |
MIM | 603725 OMIM |
HGNC | HGNC:3673 HGNC |
Ensembl | ENSG00000158815 Ensembl |
AllianceGenome | HGNC:3673 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000359441.4 | hg38 | chr8 | 22,042,820 | 22,048,809 | 5,990 |
ENST00000518533.5 | hg38 | chr8 | 22,042,398 | 22,048,806 | 6,409 |
ENST00000518533.5 | hg19 | chr8 | 21,899,909 | 21,906,317 | 6,409 |
ENST00000359441.4 | hg19 | chr8 | 21,900,331 | 21,906,320 | 5,990 |
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