TNFRSF12A TNF receptor superfamily member 12A
Information
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Benign | 0 | 2 |
| Uncertain significance | 0 | 18 |
Ranking
| ClinVar | |
|---|---|
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0 |
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0 |
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0 |
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20 |
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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
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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 | CD266 |
| SYNONYM | FN14 |
| SYNONYM | TWEAKR |
| MIM | 605914 OMIM |
| HGNC | HGNC:18152 HGNC |
| Ensembl | ENSG00000006327 Ensembl |
| AllianceGenome | HGNC:18152 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000573001.5 | hg38 | chr16 | 3,018,445 | 3,022,086 | 3,642 |
| ENST00000575124.1 | hg38 | chr16 | 3,020,375 | 3,022,383 | 2,009 |
| ENST00000326577.9 | hg38 | chr16 | 3,020,368 | 3,022,383 | 2,016 |
| ENST00000341627.5 | hg38 | chr16 | 3,020,359 | 3,022,383 | 2,025 |
| ENST00000573001.5 | hg19 | chr16 | 3,068,446 | 3,072,087 | 3,642 |
| ENST00000341627.5 | hg19 | chr16 | 3,070,360 | 3,072,384 | 2,025 |
| ENST00000326577.9 | hg19 | chr16 | 3,070,369 | 3,072,384 | 2,016 |
| ENST00000575124.1 | hg19 | chr16 | 3,070,376 | 3,072,384 | 2,009 |
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