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
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 | 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 |
Genome browser