SPATA31F3 SPATA31 subfamily F member 3
Information
- Symbol
- SPATA31F3
- Type
- protein-coding
- Description
- SPATA31 subfamily F member 3
- Entrez Gene ID
- 100129969
- Genome
- hg19
- Position
- chr9:34,889,361-34,895,719
- Genome
- hg38
- Position
- chr9:34,889,364-34,895,722
- HGNC
- HGNC:42673 HGNC
- Ensembl
- ENSG00000187791 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar |
|---|
Ranking
| ClinVar | |
|---|---|
 |
0 |
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0 |
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0 |
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0 |
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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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| 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 | FAM205C |
| SYNONYM | FAM205CP |
| HGNC | HGNC:42673 HGNC |
| Ensembl | ENSG00000187791 Ensembl |
| AllianceGenome | HGNC:42673 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000603592.1 | hg38 | chr9 | 34,889,561 | 34,895,761 | 6,201 |
| ENST00000603640.6 | hg38 | chr9 | 34,889,364 | 34,895,722 | 6,359 |
| ENST00000340783.11 | hg38 | chr9 | 34,889,066 | 34,895,764 | 6,699 |
| ENST00000340783.11 | hg19 | chr9 | 34,889,063 | 34,895,761 | 6,699 |
| ENST00000603640.6 | hg19 | chr9 | 34,889,361 | 34,895,719 | 6,359 |
| ENST00000603592.1 | hg19 | chr9 | 34,889,558 | 34,895,758 | 6,201 |
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