TNFSF14 TNF superfamily member 14
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Benign | 0 | 6 |
| Likely benign | 0 | 4 |
| Uncertain significance | 0 | 18 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
28 |
 |
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 | |||||||||||
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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| 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 | CD258 |
| SYNONYM | HVEML |
| SYNONYM | LIGHT |
| SYNONYM | LTg |
| MIM | 604520 OMIM |
| HGNC | HGNC:11930 HGNC |
| Ensembl | ENSG00000125735 Ensembl |
| AllianceGenome | HGNC:11930 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000599359.1 | hg38 | chr19 | 6,664,555 | 6,670,588 | 6,034 |
| ENST00000245912.7 | hg38 | chr19 | 6,661,253 | 6,670,117 | 8,865 |
| ENST00000675206.1 | hg38 | chr19 | 6,661,253 | 6,670,160 | 8,908 |
| ENST00000245912.7 | hg19 | chr19 | 6,661,264 | 6,670,128 | 8,865 |
| ENST00000675206.1 | hg19 | chr19 | 6,661,264 | 6,670,171 | 8,908 |
| ENST00000599359.1 | hg19 | chr19 | 6,664,566 | 6,670,599 | 6,034 |
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