TNFSF12 TNF superfamily member 12
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Benign | 0 | 26 |
| Likely benign | 0 | 176 |
| Conflicting classifications of pathogenicity | 0 | 2 |
| Uncertain significance | 0 | 224 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
34 |
 |
388 |
 |
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
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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 | |||||||||||
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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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| 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 | APO3L |
| SYNONYM | DR3LG |
| SYNONYM | TNLG4A |
| SYNONYM | TWEAK |
| MIM | 602695 OMIM |
| HGNC | HGNC:11927 HGNC |
| Ensembl | ENSG00000239697 Ensembl |
| AllianceGenome | HGNC:11927 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000700015.1 | hg38 | chr17 | 7,548,938 | 7,557,881 | 8,944 |
| ENST00000700053.1 | hg38 | chr17 | 7,549,063 | 7,557,875 | 8,813 |
| ENST00000700052.1 | hg38 | chr17 | 7,549,058 | 7,557,881 | 8,824 |
| ENST00000700051.1 | hg38 | chr17 | 7,549,058 | 7,551,779 | 2,722 |
| ENST00000293825.11 | hg38 | chr17 | 7,549,058 | 7,557,881 | 8,824 |
| ENST00000700015.1 | hg19 | chr17 | 7,452,255 | 7,461,198 | 8,944 |
| ENST00000700051.1 | hg19 | chr17 | 7,452,375 | 7,455,096 | 2,722 |
| ENST00000293825.11 | hg19 | chr17 | 7,452,375 | 7,461,198 | 8,824 |
| ENST00000700052.1 | hg19 | chr17 | 7,452,375 | 7,461,198 | 8,824 |
| ENST00000700053.1 | hg19 | chr17 | 7,452,380 | 7,461,192 | 8,813 |
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