RHOF ras homolog family member F, filopodia associated
Information
- Symbol
- RHOF
- Type
- protein-coding
- Description
- ras homolog family member F, filopodia associated
- Entrez Gene ID
- 54509
- Genome
- hg19
- Position
- chr12:122,215,660-122,231,594
- Genome
- hg38
- Position
- chr12:121,777,754-121,793,688
- MIM
- 618867 OMIM
- HGNC
- HGNC:15703 HGNC
- Ensembl
- ENSG00000139725 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Likely benign | 0 | 2 |
| Uncertain significance | 0 | 22 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
24 |
 |
0 |
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
Search Word
| 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 | |||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | Entry | Origin | Annotation | |||||||||||
Search Word
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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 | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 | ARHF |
| SYNONYM | RIF |
| MIM | 618867 OMIM |
| HGNC | HGNC:15703 HGNC |
| Ensembl | ENSG00000139725 Ensembl |
| AllianceGenome | HGNC:15703 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000537171.5 | hg38 | chr12 | 121,780,487 | 121,794,262 | 13,776 |
| ENST00000537265.5 | hg38 | chr12 | 121,779,418 | 121,793,360 | 13,943 |
| ENST00000267205.7 | hg38 | chr12 | 121,777,754 | 121,793,688 | 15,935 |
| ENST00000267205.7 | hg19 | chr12 | 122,215,660 | 122,231,594 | 15,935 |
| ENST00000537265.5 | hg19 | chr12 | 122,217,324 | 122,231,266 | 13,943 |
| ENST00000537171.5 | hg19 | chr12 | 122,218,393 | 122,232,168 | 13,776 |
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