HGF hepatocyte growth factor
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Pathogenic | 0 | 2 |
| Likely pathogenic | 0 | 2 |
| Benign | 0 | 72 |
| Likely benign | 0 | 194 |
| Conflicting classifications of pathogenicity | 0 | 24 |
| not provided | 21 | 2 |
| Uncertain significance | 0 | 162 |
Ranking
| ClinVar | |
|---|---|
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0 |
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0 |
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32 |
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388 |
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4 |
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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| Variant name | Gene | AA change | CDS | Japanese frequency |
TogoVar | MGeND | Genome | ClinVar | CIViC evidence | DisGeNET entry | COSMIC occurrence |
Prediction | |||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 | ||||||||||||||
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 | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | |||||||||||||||
| Type | ID |
|---|---|
| SYNONYM | DFNB39 |
| SYNONYM | F-TCF |
| SYNONYM | HGFB |
| SYNONYM | HPTA |
| SYNONYM | SF |
| MIM | 142409 OMIM |
| HGNC | HGNC:4893 HGNC |
| Ensembl | ENSG00000019991 Ensembl |
| AllianceGenome | HGNC:4893 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000222390.11 | hg38 | chr7 | 81,699,010 | 81,770,047 | 71,038 |
| ENST00000465234.2 | hg38 | chr7 | 81,751,916 | 81,770,024 | 18,109 |
| ENST00000423064.7 | hg38 | chr7 | 81,750,889 | 81,770,136 | 19,248 |
| ENST00000457544.7 | hg38 | chr7 | 81,702,127 | 81,770,048 | 67,922 |
| ENST00000444829.7 | hg38 | chr7 | 81,742,691 | 81,770,048 | 27,358 |
| ENST00000354224.10 | hg38 | chr7 | 81,755,121 | 81,769,971 | 14,851 |
| ENST00000643024.1 | hg38 | chr7 | 81,755,121 | 81,769,971 | 14,851 |
| ENST00000453411.6 | hg38 | chr7 | 81,742,732 | 81,770,047 | 27,316 |
| ENST00000222390.11 | hg19 | chr7 | 81,328,326 | 81,399,363 | 71,038 |
| ENST00000457544.7 | hg19 | chr7 | 81,331,443 | 81,399,364 | 67,922 |
| ENST00000444829.7 | hg19 | chr7 | 81,372,007 | 81,399,364 | 27,358 |
| ENST00000453411.6 | hg19 | chr7 | 81,372,048 | 81,399,363 | 27,316 |
| ENST00000423064.7 | hg19 | chr7 | 81,380,205 | 81,399,452 | 19,248 |
| ENST00000465234.2 | hg19 | chr7 | 81,381,232 | 81,399,340 | 18,109 |
| ENST00000354224.10 | hg19 | chr7 | 81,384,437 | 81,399,287 | 14,851 |
| ENST00000643024.1 | hg19 | chr7 | 81,384,437 | 81,399,287 | 14,851 |
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