CCDC169-SOHLH2 CCDC169-SOHLH2 readthrough
Information
- Symbol
- CCDC169-SOHLH2
- Type
- protein-coding
- Description
- CCDC169-SOHLH2 readthrough
- Entrez Gene ID
- 100526761
- Genome
- hg19
- Position
- chr13:36,742,931-36,871,979
- Genome
- hg38
- Position
- chr13:36,168,794-36,297,842
- HGNC
- HGNC:38866 HGNC
- Ensembl
- ENSG00000250709 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Benign | 0 | 6 |
| Likely benign | 0 | 22 |
| Uncertain significance | 0 | 52 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
80 |
 |
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 | C13orf38-SOHLH2 |
| SYNONYM | SOHLH2 |
| SYNONYM | TEB1 |
| HGNC | HGNC:38866 HGNC |
| Ensembl | ENSG00000250709 Ensembl |
| AllianceGenome | HGNC:38866 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000511166.1 | hg38 | chr13 | 36,168,794 | 36,297,842 | 129,049 |
| ENST00000511166.1 | hg19 | chr13 | 36,742,931 | 36,871,979 | 129,049 |
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