FGF2 fibroblast growth factor 2
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Benign | 0 | 4 |
| Likely benign | 0 | 12 |
| Uncertain significance | 0 | 28 |
Ranking
| ClinVar | |
|---|---|
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0 |
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0 |
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0 |
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42 |
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2 |
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 |
Prediction | |||||
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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 | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | ||||||||||||||
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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 | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | |||||||||||||||
| Type | ID |
|---|---|
| SYNONYM | BFGF |
| SYNONYM | FGF-2 |
| SYNONYM | FGFB |
| SYNONYM | HBGF-2 |
| MIM | 134920 OMIM |
| HGNC | HGNC:3676 HGNC |
| Ensembl | ENSG00000138685 Ensembl |
| AllianceGenome | HGNC:3676 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000608478.1 | hg38 | chr4 | 122,826,831 | 122,895,464 | 68,634 |
| ENST00000644866.2 | hg38 | chr4 | 122,826,831 | 122,898,236 | 71,406 |
| ENST00000264498.9 | hg38 | chr4 | 122,826,682 | 122,898,236 | 71,555 |
| ENST00000264498.9 | hg19 | chr4 | 123,747,837 | 123,819,391 | 71,555 |
| ENST00000608478.1 | hg19 | chr4 | 123,747,986 | 123,816,619 | 68,634 |
| ENST00000644866.2 | hg19 | chr4 | 123,747,986 | 123,819,391 | 71,406 |
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