TMSB15B thymosin beta 15B
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| not provided | 6 | 0 |
| Uncertain significance | 0 | 6 |
Ranking
| ClinVar | |
|---|---|
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0 |
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0 |
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0 |
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6 |
 |
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
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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 | TMSB15A |
| SYNONYM | TMSL8 |
| SYNONYM | TMSNB |
| SYNONYM | Tbeta15b |
| MIM | 301011 OMIM |
| HGNC | HGNC:28612 HGNC |
| Ensembl | ENSG00000158427 Ensembl |
| AllianceGenome | HGNC:28612 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000540220.6 | hg38 | chrX | 103,962,627 | 103,965,976 | 3,350 |
| ENST00000563257.5 | hg38 | chrX | 103,962,641 | 103,966,712 | 4,072 |
| ENST00000569577.1 | hg38 | chrX | 103,962,675 | 103,965,968 | 3,294 |
| ENST00000436583.5 | hg38 | chrX | 103,962,669 | 103,965,981 | 3,313 |
| ENST00000419165.5 | hg38 | chrX | 103,918,896 | 103,965,987 | 47,092 |
| ENST00000419165.5 | hg19 | chrX | 103,173,479 | 103,220,560 | 47,082 |
| ENST00000540220.6 | hg19 | chrX | 103,217,200 | 103,220,549 | 3,350 |
| ENST00000563257.5 | hg19 | chrX | 103,217,214 | 103,221,285 | 4,072 |
| ENST00000436583.5 | hg19 | chrX | 103,217,242 | 103,220,554 | 3,313 |
| ENST00000569577.1 | hg19 | chrX | 103,217,248 | 103,220,541 | 3,294 |
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