RANGRF RAN guanine nucleotide release factor
Information
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Benign | 0 | 14 |
| Likely benign | 0 | 124 |
| Conflicting classifications of pathogenicity | 0 | 2 |
| Uncertain significance | 0 | 156 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
44 |
 |
248 |
 |
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
| Target data | : |
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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| Category | : |
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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 | HSPC165 |
| SYNONYM | HSPC236 |
| SYNONYM | MOG1 |
| SYNONYM | RANGNRF |
| MIM | 607954 OMIM |
| HGNC | HGNC:17679 HGNC |
| Ensembl | ENSG00000108961 Ensembl |
| AllianceGenome | HGNC:17679 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000439238.3 | hg38 | chr17 | 8,288,678 | 8,290,092 | 1,415 |
| ENST00000580434.5 | hg38 | chr17 | 8,288,671 | 8,290,092 | 1,422 |
| ENST00000407006.8 | hg38 | chr17 | 8,288,654 | 8,290,090 | 1,437 |
| ENST00000226105.11 | hg38 | chr17 | 8,288,670 | 8,290,087 | 1,418 |
| ENST00000407006.8 | hg19 | chr17 | 8,191,972 | 8,193,408 | 1,437 |
| ENST00000226105.11 | hg19 | chr17 | 8,191,988 | 8,193,405 | 1,418 |
| ENST00000580434.5 | hg19 | chr17 | 8,191,989 | 8,193,410 | 1,422 |
| ENST00000439238.3 | hg19 | chr17 | 8,191,996 | 8,193,410 | 1,415 |
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