TMEM198 transmembrane protein 198
Information
- Symbol
- TMEM198
- Type
- protein-coding
- Description
- transmembrane protein 198
- Entrez Gene ID
- 130612
- Genome
- hg19
- Position
- chr2:220,408,385-220,415,301
- Genome
- hg38
- Position
- chr2:219,543,663-219,550,579
- HGNC
- HGNC:33704 HGNC
- Ensembl
- ENSG00000188760 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Uncertain significance | 0 | 44 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
44 |
 |
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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| 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 | TMEM198A |
| HGNC | HGNC:33704 HGNC |
| Ensembl | ENSG00000188760 Ensembl |
| AllianceGenome | HGNC:33704 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000344458.6 | hg38 | chr2 | 219,543,663 | 219,550,579 | 6,917 |
| ENST00000373883.4 | hg38 | chr2 | 219,544,028 | 219,550,595 | 6,568 |
| ENST00000344458.6 | hg19 | chr2 | 220,408,385 | 220,415,301 | 6,917 |
| ENST00000373883.4 | hg19 | chr2 | 220,408,750 | 220,415,317 | 6,568 |
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