FGF6 fibroblast growth factor 6
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 2 |
Likely benign | 0 | 4 |
not provided | 1 | 0 |
Uncertain significance | 0 | 20 |
Ranking
ClinVar | |
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0 |
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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
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HGVD
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TOMMO
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Disease area statistics
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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 | HBGF-6 |
SYNONYM | HST2 |
MIM | 134921 OMIM |
HGNC | HGNC:3684 HGNC |
Ensembl | ENSG00000111241 Ensembl |
AllianceGenome | HGNC:3684 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000228837.3 | hg38 | chr12 | 4,434,142 | 4,445,815 | 11,674 |
ENST00000228837.3 | hg19 | chr12 | 4,543,308 | 4,554,981 | 11,674 |
Key | Value |
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strand | - |
UniProt | OG |
start | 4,543,307 |
Gene Symbol | FGF6 |
Entrez GeneId | 2,251 |
Chr Band | 12p13 |
end | 4,554,779 |
chr | chr12 |
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