FRS2 fibroblast growth factor receptor substrate 2
Information
- Symbol
- FRS2
- Type
- protein-coding
- Description
- fibroblast growth factor receptor substrate 2
- Entrez Gene ID
- 10818
- Genome
- hg19
- Position
- chr12:69,864,168-69,973,573
- Genome
- hg38
- Position
- chr12:69,470,388-69,579,793
- MIM
- 607743 OMIM
- HGNC
- HGNC:16971 HGNC
- Ensembl
- ENSG00000166225 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| not provided | 1 | 0 |
| Uncertain significance | 0 | 54 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
54 |
 |
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
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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| Filtering | : |
| 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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| Filtering | : |
| 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 | FRS1A |
| SYNONYM | FRS2A |
| SYNONYM | FRS2alpha |
| SYNONYM | SNT |
| SYNONYM | SNT-1 |
| SYNONYM | SNT1 |
| MIM | 607743 OMIM |
| HGNC | HGNC:16971 HGNC |
| Ensembl | ENSG00000166225 Ensembl |
| AllianceGenome | HGNC:16971 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000397997.6 | hg38 | chr12 | 69,557,789 | 69,579,789 | 22,001 |
| ENST00000549921.6 | hg38 | chr12 | 69,470,388 | 69,579,793 | 109,406 |
| ENST00000550389.5 | hg38 | chr12 | 69,470,406 | 69,579,782 | 109,377 |
| ENST00000549921.6 | hg19 | chr12 | 69,864,168 | 69,973,573 | 109,406 |
| ENST00000550389.5 | hg19 | chr12 | 69,864,186 | 69,973,562 | 109,377 |
| ENST00000397997.6 | hg19 | chr12 | 69,951,569 | 69,973,569 | 22,001 |
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