APOA2 apolipoprotein A2
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Pathogenic | 0 | 2 |
Likely pathogenic | 0 | 2 |
Benign | 0 | 8 |
Likely benign | 0 | 6 |
Uncertain significance | 0 | 18 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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8 |
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24 |
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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 |
Type | ID |
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SYNONYM | Apo-AII |
SYNONYM | ApoA-II |
SYNONYM | apoAII |
MIM | 107670 OMIM |
HGNC | HGNC:601 HGNC |
Ensembl | ENSG00000158874 Ensembl |
AllianceGenome | HGNC:601 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000468465.5 | hg38 | chr1 | 161,222,292 | 161,223,631 | 1,340 |
ENST00000367990.7 | hg38 | chr1 | 161,222,292 | 161,223,628 | 1,337 |
ENST00000491350.1 | hg38 | chr1 | 161,222,319 | 161,223,408 | 1,090 |
ENST00000464492.5 | hg38 | chr1 | 161,222,316 | 161,223,615 | 1,300 |
ENST00000463812.1 | hg38 | chr1 | 161,222,292 | 161,223,631 | 1,340 |
ENST00000470459.6 | hg38 | chr1 | 161,222,296 | 161,223,628 | 1,333 |
ENST00000367990.7 | hg19 | chr1 | 161,192,082 | 161,193,418 | 1,337 |
ENST00000463812.1 | hg19 | chr1 | 161,192,082 | 161,193,421 | 1,340 |
ENST00000468465.5 | hg19 | chr1 | 161,192,082 | 161,193,421 | 1,340 |
ENST00000470459.6 | hg19 | chr1 | 161,192,086 | 161,193,418 | 1,333 |
ENST00000464492.5 | hg19 | chr1 | 161,192,106 | 161,193,405 | 1,300 |
ENST00000491350.1 | hg19 | chr1 | 161,192,109 | 161,193,198 | 1,090 |
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