TPSG1 tryptase gamma 1
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 4 |
Likely benign | 0 | 16 |
not provided | 2 | 0 |
Uncertain significance | 0 | 74 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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94 |
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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
Locus Zoom
Variants
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Target data | : |
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Variant name | Gene | AA change | CDS | Japanese frequency |
TogoVar | MGeND | Genome | ClinVar | CIViC evidence | DisGeNET entry | COSMIC occurrence |
Prediction | |||||
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Entry | Origin | Type | Annotation | Entry | Origin | Annotation |
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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 | |||
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Entry | Origin | Type | Annotation |
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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 | |||
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Entry | Origin | Type | Annotation |
Type | ID |
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SYNONYM | PRSS31 |
SYNONYM | TMT |
SYNONYM | trpA |
MIM | 609341 OMIM |
HGNC | HGNC:14134 HGNC |
Ensembl | ENSG00000116176 Ensembl |
AllianceGenome | HGNC:14134 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000711428.1 | hg38 | chr16 | 1,221,655 | 1,225,793 | 4,139 |
ENST00000711429.1 | hg38 | chr16 | 1,221,746 | 1,225,289 | 3,544 |
ENST00000234798.5 | hg38 | chr16 | 1,221,651 | 1,225,268 | 3,618 |
ENST00000234798.5 | hg19 | chr16 | 1,271,651 | 1,275,268 | 3,618 |
ENST00000711428.1 | hg19 | chr16 | 1,271,655 | 1,275,793 | 4,139 |
ENST00000711429.1 | hg19 | chr16 | 1,271,746 | 1,275,289 | 3,544 |
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