TNFSF13 TNF superfamily member 13
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Benign | 0 | 8 |
| Uncertain significance | 0 | 16 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
6 |
 |
18 |
 |
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
|
| Category | : |
|
| Search word | : | |
| Filtering | : |
| 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
|
| Category | : |
|
| Search word | : | |
| 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
|
| Category | : |
|
| 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 | |||||||||||||||
| Type | ID |
|---|---|
| SYNONYM | APRIL |
| SYNONYM | CD256 |
| SYNONYM | TALL-2 |
| SYNONYM | TALL2 |
| SYNONYM | TNLG7B |
| SYNONYM | TRDL-1 |
| SYNONYM | UNQ383/PRO715 |
| SYNONYM | ZTNF2 |
| MIM | 604472 OMIM |
| HGNC | HGNC:11928 HGNC |
| Ensembl | ENSG00000161955 Ensembl |
| AllianceGenome | HGNC:11928 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000380535.8 | hg38 | chr17 | 7,558,292 | 7,561,608 | 3,317 |
| ENST00000349228.8 | hg38 | chr17 | 7,558,476 | 7,561,600 | 3,125 |
| ENST00000396545.4 | hg38 | chr17 | 7,558,787 | 7,561,601 | 2,815 |
| ENST00000396542.5 | hg38 | chr17 | 7,558,293 | 7,560,835 | 2,543 |
| ENST00000625791.2 | hg38 | chr17 | 7,558,759 | 7,560,838 | 2,080 |
| ENST00000483039.5 | hg38 | chr17 | 7,558,292 | 7,561,292 | 3,001 |
| ENST00000338784.9 | hg38 | chr17 | 7,558,750 | 7,561,601 | 2,852 |
| ENST00000483039.5 | hg19 | chr17 | 7,461,609 | 7,464,609 | 3,001 |
| ENST00000380535.8 | hg19 | chr17 | 7,461,609 | 7,464,925 | 3,317 |
| ENST00000396542.5 | hg19 | chr17 | 7,461,610 | 7,464,152 | 2,543 |
| ENST00000349228.8 | hg19 | chr17 | 7,461,793 | 7,464,917 | 3,125 |
| ENST00000338784.9 | hg19 | chr17 | 7,462,067 | 7,464,918 | 2,852 |
| ENST00000625791.2 | hg19 | chr17 | 7,462,076 | 7,464,155 | 2,080 |
| ENST00000396545.4 | hg19 | chr17 | 7,462,104 | 7,464,918 | 2,815 |
Genome browser