PGC progastricsin
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 6 |
Uncertain significance | 0 | 50 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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56 |
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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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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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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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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 | PEPC |
SYNONYM | PGII |
MIM | 169740 OMIM |
HGNC | HGNC:8890 HGNC |
Ensembl | ENSG00000096088 Ensembl |
AllianceGenome | HGNC:8890 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000425343.6 | hg38 | chr6 | 41,740,838 | 41,747,401 | 6,564 |
ENST00000373025.7 | hg38 | chr6 | 41,736,711 | 41,747,397 | 10,687 |
ENST00000373025.7 | hg19 | chr6 | 41,704,449 | 41,715,135 | 10,687 |
ENST00000425343.6 | hg19 | chr6 | 41,708,576 | 41,715,139 | 6,564 |
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