TTC31 tetratricopeptide repeat domain 31
Information
- Symbol
- TTC31
- Type
- protein-coding
- Description
- tetratricopeptide repeat domain 31
- Entrez Gene ID
- 64427
- Genome
- hg19
- Position
- chr2:74,710,208-74,721,686
- Genome
- hg38
- Position
- chr2:74,483,081-74,494,559
- HGNC
- HGNC:25759 HGNC
- Ensembl
- ENSG00000115282 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Likely benign | 0 | 2 |
| Uncertain significance | 0 | 74 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
76 |
 |
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 | |||||||||||||||
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000233623.11 | hg38 | chr2 | 74,483,081 | 74,494,559 | 11,479 |
| ENST00000442235.6 | hg38 | chr2 | 74,483,087 | 74,493,083 | 9,997 |
| ENST00000410003.5 | hg38 | chr2 | 74,483,087 | 74,494,559 | 11,473 |
| ENST00000233623.11 | hg19 | chr2 | 74,710,208 | 74,721,686 | 11,479 |
| ENST00000442235.6 | hg19 | chr2 | 74,710,214 | 74,720,210 | 9,997 |
| ENST00000410003.5 | hg19 | chr2 | 74,710,214 | 74,721,686 | 11,473 |
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