FLCN folliculin
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Pathogenic | 9 | 612 |
Likely pathogenic | 1 | 152 |
Benign | 4 | 186 |
Likely benign | 1 | 1,478 |
Conflicting classifications of pathogenicity | 0 | 370 |
not provided | 8 | 2 |
Uncertain significance | 16 | 1,832 |
Ranking
ClinVar | |
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0 |
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0 |
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1,526 |
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2,498 |
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98 |
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
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 |
Search Word
Target data | : |
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 | BHD |
SYNONYM | DENND8B |
SYNONYM | FLCL |
MIM | 607273 OMIM |
HGNC | HGNC:27310 HGNC |
Ensembl | ENSG00000154803 Ensembl |
AllianceGenome | HGNC:27310 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000389169.9 | hg38 | chr17 | 17,221,171 | 17,237,139 | 15,969 |
ENST00000285071.9 | hg38 | chr17 | 17,212,212 | 17,237,168 | 24,957 |
ENST00000285071.9 | hg19 | chr17 | 17,115,526 | 17,140,482 | 24,957 |
ENST00000389169.9 | hg19 | chr17 | 17,124,485 | 17,140,453 | 15,969 |
Key | Value |
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strand | - |
UniProt | TSG |
start | 17,115,526 |
Gene Symbol | FLCN |
Entrez GeneId | 201,163 |
Chr Band | 17p11.2 |
end | 17,140,501 |
chr | chr17 |
Name | folliculin |
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