APOL3 apolipoprotein L3
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 12 |
Likely benign | 0 | 10 |
Uncertain significance | 0 | 50 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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2 |
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70 |
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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
Search Word
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 | APOLIII |
SYNONYM | CG121 |
SYNONYM | CG12_1 |
SYNONYM | apoL-III |
MIM | 607253 OMIM |
HGNC | HGNC:14868 HGNC |
Ensembl | ENSG00000128284 Ensembl |
AllianceGenome | HGNC:14868 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000424878.4 | hg38 | chr22 | 36,140,329 | 36,160,755 | 20,427 |
ENST00000397287.6 | hg38 | chr22 | 36,140,330 | 36,166,177 | 25,848 |
ENST00000361710.6 | hg38 | chr22 | 36,140,330 | 36,166,177 | 25,848 |
ENST00000397293.6 | hg38 | chr22 | 36,140,330 | 36,160,929 | 20,600 |
ENST00000349314.6 | hg38 | chr22 | 36,140,330 | 36,160,929 | 20,600 |
ENST00000349314.6 | hg19 | chr22 | 36,536,378 | 36,556,977 | 20,600 |
ENST00000397293.6 | hg19 | chr22 | 36,536,378 | 36,556,977 | 20,600 |
ENST00000424878.4 | hg19 | chr22 | 36,536,377 | 36,556,803 | 20,427 |
ENST00000361710.6 | hg19 | chr22 | 36,536,378 | 36,562,225 | 25,848 |
ENST00000397287.6 | hg19 | chr22 | 36,536,378 | 36,562,225 | 25,848 |
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