SNRPF small nuclear ribonucleoprotein polypeptide F
Information
- Symbol
- SNRPF
- Type
- protein-coding
- Description
- small nuclear ribonucleoprotein polypeptide F
- Entrez Gene ID
- 6636
- Genome
- hg19
- Position
- chr12:96,252,730-96,259,918
- Genome
- hg38
- Position
- chr12:95,858,952-95,866,140
- MIM
- 603541 OMIM
- HGNC
- HGNC:11162 HGNC
- Ensembl
- ENSG00000139343 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Likely benign | 0 | 6 |
| Uncertain significance | 0 | 64 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
70 |
 |
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
|
| Category | : |
|
| Search word | : | |
| Filtering | : |
| 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
|
| Category | : |
|
| Search word | : | |
| 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
|
| Category | : |
|
| Search word | : | |
| 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 | SMF |
| SYNONYM | Sm-F |
| SYNONYM | snRNP-F |
| MIM | 603541 OMIM |
| HGNC | HGNC:11162 HGNC |
| Ensembl | ENSG00000139343 Ensembl |
| AllianceGenome | HGNC:11162 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000552085.1 | hg38 | chr12 | 95,858,969 | 95,903,828 | 44,860 |
| ENST00000553192.5 | hg38 | chr12 | 95,858,965 | 95,880,001 | 21,037 |
| ENST00000266735.10 | hg38 | chr12 | 95,858,952 | 95,866,140 | 7,189 |
| ENST00000266735.10 | hg19 | chr12 | 96,252,730 | 96,259,918 | 7,189 |
| ENST00000553192.5 | hg19 | chr12 | 96,252,743 | 96,273,779 | 21,037 |
| ENST00000552085.1 | hg19 | chr12 | 96,252,747 | 96,297,606 | 44,860 |
Genome browser