PON2 paraoxonase 2
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 38 |
Likely benign | 0 | 32 |
Uncertain significance | 0 | 42 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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6 |
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102 |
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2 |
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 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000633531.1 | hg38 | chr7 | 95,404,863 | 95,435,072 | 30,210 |
ENST00000633192.1 | hg38 | chr7 | 95,404,897 | 95,435,329 | 30,433 |
ENST00000433091.6 | hg38 | chr7 | 95,404,880 | 95,435,198 | 30,319 |
ENST00000222572.8 | hg38 | chr7 | 95,404,862 | 95,435,028 | 30,167 |
ENST00000222572.8 | hg19 | chr7 | 95,034,174 | 95,064,340 | 30,167 |
ENST00000433091.6 | hg19 | chr7 | 95,034,192 | 95,064,510 | 30,319 |
ENST00000633192.1 | hg19 | chr7 | 95,034,209 | 95,064,641 | 30,433 |
ENST00000633531.1 | hg19 | chr7 | 95,034,175 | 95,064,384 | 30,210 |
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