TNFRSF19 TNF receptor superfamily member 19
Information
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Benign | 0 | 2 |
| Likely benign | 0 | 8 |
| not provided | 1 | 0 |
| Uncertain significance | 0 | 42 |
Ranking
| ClinVar | |
|---|---|
![]() |
0 |
![]() |
0 |
![]() |
0 |
![]() |
52 |
![]() |
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
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 | TAJ |
| SYNONYM | TAJ-alpha |
| SYNONYM | TRADE |
| SYNONYM | TROY |
| MIM | 606122 OMIM |
| HGNC | HGNC:11915 HGNC |
| Ensembl | ENSG00000127863 Ensembl |
| AllianceGenome | HGNC:11915 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000403372.6 | hg38 | chr13 | 23,570,370 | 23,676,104 | 105,735 |
| ENST00000382258.8 | hg38 | chr13 | 23,579,360 | 23,669,273 | 89,914 |
| ENST00000248484.9 | hg38 | chr13 | 23,570,412 | 23,676,093 | 105,682 |
| ENST00000382263.3 | hg38 | chr13 | 23,579,380 | 23,676,093 | 96,714 |
| ENST00000403372.6 | hg19 | chr13 | 24,144,509 | 24,250,243 | 105,735 |
| ENST00000248484.9 | hg19 | chr13 | 24,144,551 | 24,250,232 | 105,682 |
| ENST00000382258.8 | hg19 | chr13 | 24,153,499 | 24,243,412 | 89,914 |
| ENST00000382263.3 | hg19 | chr13 | 24,153,519 | 24,250,232 | 96,714 |
Genome browser




