TNRC18 trinucleotide repeat containing 18
Information
- Symbol
- TNRC18
- Type
- protein-coding
- Description
- trinucleotide repeat containing 18
- Entrez Gene ID
- 84629
- Genome
- hg19
- Position
- chr7:5,346,442-5,463,465
- Genome
- hg38
- Position
- chr7:5,306,811-5,423,834
- HGNC
- HGNC:11962 HGNC
- Ensembl
- ENSG00000182095 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Benign | 0 | 242 |
| Likely benign | 0 | 134 |
| Conflicting classifications of pathogenicity | 0 | 4 |
| Uncertain significance | 0 | 600 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
24 |
 |
938 |
 |
2 |
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 | CAGL79 |
| SYNONYM | TNRC18A |
| HGNC | HGNC:11962 HGNC |
| Ensembl | ENSG00000182095 Ensembl |
| AllianceGenome | HGNC:11962 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000430969.6 | hg38 | chr7 | 5,306,811 | 5,423,834 | 117,024 |
| ENST00000399434.2 | hg38 | chr7 | 5,389,450 | 5,425,414 | 35,965 |
| ENST00000399537.8 | hg38 | chr7 | 5,306,790 | 5,423,546 | 116,757 |
| ENST00000399537.8 | hg19 | chr7 | 5,346,421 | 5,463,177 | 116,757 |
| ENST00000430969.6 | hg19 | chr7 | 5,346,442 | 5,463,465 | 117,024 |
| ENST00000399434.2 | hg19 | chr7 | 5,429,081 | 5,465,045 | 35,965 |
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