LITAFD LITAF domain containing
Information
- Symbol
- LITAFD
- Type
- protein-coding
- Description
- LITAF domain containing
- Entrez Gene ID
- 101929989
- Genome
- hg19
- Position
- chr16:8,976,332-8,979,208
- Genome
- hg38
- Position
- chr16:8,882,475-8,885,351
- HGNC
- HGNC:53927 HGNC
- Ensembl
- ENSG00000283516 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Benign | 0 | 2 |
| Likely benign | 0 | 2 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
4 |
 |
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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| Category | : |
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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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| Search word | : | |
| 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 |
|---|---|---|---|---|---|
| ENST00000637237.1 | hg38 | chr16 | 8,882,475 | 8,885,351 | 2,877 |
| ENST00000637929.1 | hg38 | chr16 | 8,882,698 | 8,885,179 | 2,482 |
| ENST00000636296.2 | hg38 | chr16 | 8,882,351 | 8,885,350 | 3,000 |
| ENST00000636296.2 | hg19 | chr16 | 8,976,208 | 8,979,207 | 3,000 |
| ENST00000637237.1 | hg19 | chr16 | 8,976,332 | 8,979,208 | 2,877 |
| ENST00000637929.1 | hg19 | chr16 | 8,976,555 | 8,979,036 | 2,482 |
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