APOC3 apolipoprotein C3
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Pathogenic | 0 | 4 |
Benign | 0 | 32 |
Likely benign | 0 | 42 |
Conflicting classifications of pathogenicity | 0 | 8 |
Uncertain significance | 0 | 42 |
Ranking
ClinVar | |
---|---|
![]() |
0 |
![]() |
0 |
![]() |
20 |
![]() |
86 |
![]() |
6 |
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
|
Category | : |
|
Search word | : | |
Filtering | : |
Variant name | Gene | AA change | CDS | Japanese frequency |
TogoVar | MGeND | Genome | ClinVar | CIViC evidence | DisGeNET entry | COSMIC occurrence |
Prediction | |||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Entry | Origin | Type | Annotation | Entry | Origin | Annotation |
Search Word
Target data | : |
MGeND data only
|
Category | : |
|
Search word | : | |
Filtering | : |
Name | MGeND | Type | Genome | Size | Chromosome | Start | Stop | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Entry | Origin | Type | Annotation |
Search Word
Target data | : |
MGeND data only
|
Category | : |
|
Search word | : | |
Filtering | : |
Name | MGeND | Type | Genome | Gene symbol | Chromosome | Genomic start | Genomic stop | Strand | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Entry | Origin | Type | Annotation |
Type | ID |
---|---|
SYNONYM | APOCIII |
SYNONYM | Apo-C3 |
SYNONYM | ApoC-3 |
MIM | 107720 OMIM |
HGNC | HGNC:610 HGNC |
Ensembl | ENSG00000110245 Ensembl |
AllianceGenome | HGNC:610 |
Descrption | Source | Links |
---|
ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000630701.1 | hg38 | chr11 | 116,830,529 | 116,833,071 | 2,543 |
ENST00000227667.8 | hg38 | chr11 | 116,829,907 | 116,833,072 | 3,166 |
ENST00000375345.3 | hg38 | chr11 | 116,829,915 | 116,833,072 | 3,158 |
ENST00000227667.8 | hg19 | chr11 | 116,700,623 | 116,703,788 | 3,166 |
ENST00000375345.3 | hg19 | chr11 | 116,700,631 | 116,703,788 | 3,158 |
ENST00000630701.1 | hg19 | chr11 | 116,701,245 | 116,703,787 | 2,543 |
Genome browser