PGA3 pepsinogen A3
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 6 |
Uncertain significance | 0 | 12 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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18 |
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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 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000325558.11 | hg38 | chr11 | 61,203,515 | 61,213,098 | 9,584 |
ENST00000543125.5 | hg38 | chr11 | 61,209,548 | 61,212,865 | 3,318 |
ENST00000538258.1 | hg38 | chr11 | 61,210,754 | 61,212,839 | 2,086 |
ENST00000325558.11 | hg19 | chr11 | 60,970,987 | 60,980,570 | 9,584 |
ENST00000543125.5 | hg19 | chr11 | 60,977,020 | 60,980,337 | 3,318 |
ENST00000538258.1 | hg19 | chr11 | 60,978,226 | 60,980,311 | 2,086 |
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