PRTN3 proteinase 3
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 4 |
Likely benign | 0 | 12 |
Uncertain significance | 0 | 24 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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2 |
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36 |
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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
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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 | ACPA |
SYNONYM | AGP7 |
SYNONYM | C-ANCA |
SYNONYM | CANCA |
SYNONYM | MBN |
SYNONYM | MBT |
SYNONYM | NP-4 |
SYNONYM | NP4 |
SYNONYM | P29 |
SYNONYM | PR-3 |
SYNONYM | PR3 |
MIM | 177020 OMIM |
HGNC | HGNC:9495 HGNC |
Ensembl | ENSG00000196415 Ensembl |
AllianceGenome | HGNC:9495 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000544537.2 | hg38 | chr19 | 843,341 | 848,175 | 4,835 |
ENST00000234347.10 | hg38 | chr19 | 840,999 | 848,175 | 7,177 |
ENST00000234347.10 | hg19 | chr19 | 840,999 | 848,175 | 7,177 |
ENST00000544537.2 | hg19 | chr19 | 843,341 | 848,175 | 4,835 |
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