SWSAP1 SWIM-type zinc finger 7 associated protein 1
Information
- Symbol
- SWSAP1
- Type
- protein-coding
- Description
- SWIM-type zinc finger 7 associated protein 1
- Entrez Gene ID
- 126074
- Genome
- hg19
- Position
- chr19:11,485,342-11,486,845
- Genome
- hg38
- Position
- chr19:11,374,666-11,376,169
- MIM
- 614536 OMIM
- HGNC
- HGNC:26638 HGNC
- Ensembl
- ENSG00000173928 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Likely benign | 0 | 2 |
| Uncertain significance | 0 | 14 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
16 |
 |
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 | C19orf39 |
| SYNONYM | SWS1AP1 |
| SYNONYM | ZSWIM7AP1 |
| MIM | 614536 OMIM |
| HGNC | HGNC:26638 HGNC |
| Ensembl | ENSG00000173928 Ensembl |
| AllianceGenome | HGNC:26638 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000312423.4 | hg38 | chr19 | 11,374,707 | 11,376,951 | 2,245 |
| ENST00000674460.1 | hg38 | chr19 | 11,374,666 | 11,376,169 | 1,504 |
| ENST00000674460.1 | hg19 | chr19 | 11,485,342 | 11,486,845 | 1,504 |
| ENST00000312423.4 | hg19 | chr19 | 11,485,383 | 11,487,627 | 2,245 |
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