APOC2 apolipoprotein C2
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Pathogenic | 0 | 26 |
Likely pathogenic | 0 | 4 |
Benign | 0 | 28 |
Likely benign | 0 | 82 |
Conflicting classifications of pathogenicity | 0 | 12 |
Uncertain significance | 0 | 66 |
Ranking
ClinVar | |
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0 |
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0 |
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28 |
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152 |
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16 |
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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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-CII |
SYNONYM | APOC-II |
MIM | 608083 OMIM |
HGNC | HGNC:609 HGNC |
Ensembl | ENSG00000234906 Ensembl |
AllianceGenome | HGNC:609 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000591597.5 | hg38 | chr19 | 44,946,056 | 44,949,399 | 3,344 |
ENST00000585786.1 | hg38 | chr19 | 44,948,286 | 44,949,332 | 1,047 |
ENST00000592257.5 | hg38 | chr19 | 44,946,035 | 44,949,395 | 3,361 |
ENST00000252490.7 | hg38 | chr19 | 44,946,051 | 44,949,565 | 3,515 |
ENST00000590360.2 | hg38 | chr19 | 44,947,203 | 44,949,565 | 2,363 |
ENST00000592257.5 | hg19 | chr19 | 45,449,292 | 45,452,652 | 3,361 |
ENST00000252490.7 | hg19 | chr19 | 45,449,308 | 45,452,822 | 3,515 |
ENST00000591597.5 | hg19 | chr19 | 45,449,313 | 45,452,656 | 3,344 |
ENST00000590360.2 | hg19 | chr19 | 45,450,460 | 45,452,822 | 2,363 |
ENST00000585786.1 | hg19 | chr19 | 45,451,543 | 45,452,589 | 1,047 |
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