TAF10 TATA-box binding protein associated factor 10
Information
- Symbol
- TAF10
- Type
- protein-coding
- Description
- TATA-box binding protein associated factor 10
- Entrez Gene ID
- 6881
- Genome
- hg19
- Position
- chr11:6,627,524-6,633,447
- Genome
- hg38
- Position
- chr11:6,606,294-6,612,216
- MIM
- 600475 OMIM
- HGNC
- HGNC:11543 HGNC
- Ensembl
- ENSG00000166337 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Benign | 0 | 38 |
| Likely benign | 0 | 302 |
| Conflicting classifications of pathogenicity | 0 | 16 |
| Uncertain significance | 0 | 420 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
188 |
 |
544 |
 |
8 |
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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| 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 | TAF2A |
| SYNONYM | TAF2H |
| SYNONYM | TAFII30 |
| MIM | 600475 OMIM |
| HGNC | HGNC:11543 HGNC |
| Ensembl | ENSG00000166337 Ensembl |
| AllianceGenome | HGNC:11543 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000527248.3 | hg38 | chr11 | 6,610,845 | 6,612,189 | 1,345 |
| ENST00000299424.9 | hg38 | chr11 | 6,606,294 | 6,612,216 | 5,923 |
| ENST00000299424.9 | hg19 | chr11 | 6,627,524 | 6,633,447 | 5,924 |
| ENST00000527248.3 | hg19 | chr11 | 6,632,076 | 6,633,420 | 1,345 |
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