PRSS1 serine protease 1
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Pathogenic | 4 | 16 |
Likely pathogenic | 0 | 10 |
Benign | 10 | 68 |
Likely benign | 1 | 438 |
Conflicting classifications of pathogenicity | 0 | 54 |
Uncertain significance | 8 | 798 |
Ranking
ClinVar | |
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0 |
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0 |
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354 |
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926 |
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10 |
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 | |||||
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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 | TRP1 |
SYNONYM | TRY1 |
SYNONYM | TRY4 |
SYNONYM | TRYP1 |
MIM | 276000 OMIM |
HGNC | HGNC:9475 HGNC |
Ensembl | ENSG00000204983 Ensembl |
AllianceGenome | HGNC:9475 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000486171.5 | hg38 | chr7 | 142,749,468 | 142,753,020 | 3,553 |
ENST00000492062.2 | hg38 | chr7 | 142,749,472 | 142,753,069 | 3,598 |
ENST00000311737.12 | hg38 | chr7 | 142,749,472 | 142,753,072 | 3,601 |
ENST00000486171.5 | hg19 | chr7 | 142,457,319 | 142,460,871 | 3,553 |
ENST00000492062.2 | hg19 | chr7 | 142,457,323 | 142,460,920 | 3,598 |
ENST00000311737.12 | hg19 | chr7 | 142,457,323 | 142,460,923 | 3,601 |
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