AGT angiotensinogen
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Pathogenic | 4 | 12 |
Likely pathogenic | 0 | 10 |
Benign | 0 | 66 |
Likely benign | 0 | 148 |
Conflicting classifications of pathogenicity | 0 | 30 |
Uncertain significance | 0 | 180 |
Ranking
ClinVar | |
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0 |
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0 |
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84 |
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308 |
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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
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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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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 | ANHU |
SYNONYM | SERPINA8 |
SYNONYM | hFLT1 |
MIM | 106150 OMIM |
HGNC | HGNC:333 HGNC |
Ensembl | ENSG00000135744 Ensembl |
AllianceGenome | HGNC:333 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000681514.1 | hg38 | chr1 | 230,702,155 | 230,714,122 | 11,968 |
ENST00000366667.6 | hg38 | chr1 | 230,702,523 | 230,714,122 | 11,600 |
ENST00000681269.1 | hg38 | chr1 | 230,702,523 | 230,745,576 | 43,054 |
ENST00000679684.1 | hg38 | chr1 | 230,703,767 | 230,714,566 | 10,800 |
ENST00000680041.1 | hg38 | chr1 | 230,702,155 | 230,714,145 | 11,991 |
ENST00000679957.1 | hg38 | chr1 | 230,703,141 | 230,714,566 | 11,426 |
ENST00000680783.1 | hg38 | chr1 | 230,690,776 | 230,714,566 | 23,791 |
ENST00000680783.1 | hg19 | chr1 | 230,826,522 | 230,850,312 | 23,791 |
ENST00000681514.1 | hg19 | chr1 | 230,837,901 | 230,849,868 | 11,968 |
ENST00000680041.1 | hg19 | chr1 | 230,837,901 | 230,849,891 | 11,991 |
ENST00000366667.6 | hg19 | chr1 | 230,838,269 | 230,849,868 | 11,600 |
ENST00000681269.1 | hg19 | chr1 | 230,838,269 | 230,881,322 | 43,054 |
ENST00000679957.1 | hg19 | chr1 | 230,838,887 | 230,850,312 | 11,426 |
ENST00000679684.1 | hg19 | chr1 | 230,839,513 | 230,850,312 | 10,800 |
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