APOC1 apolipoprotein C1
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Likely benign | 0 | 2 |
| Uncertain significance | 0 | 6 |
Ranking
| ClinVar | |
|---|---|
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0 |
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0 |
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0 |
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8 |
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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 | |||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | Entry | Origin | Annotation | |||||||||||
Search Word
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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 | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | ||||||||||||||
Search Word
| 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 | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | |||||||||||||||
| Type | ID |
|---|---|
| SYNONYM | APOC1B |
| SYNONYM | Apo-CI |
| SYNONYM | ApoC-I |
| SYNONYM | apo-CIB |
| SYNONYM | apoC-IB |
| MIM | 107710 OMIM |
| HGNC | HGNC:607 HGNC |
| Ensembl | ENSG00000130208 Ensembl |
| AllianceGenome | HGNC:607 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000592885.5 | hg38 | chr19 | 44,914,703 | 44,919,344 | 4,642 |
| ENST00000589781.1 | hg38 | chr19 | 44,914,710 | 44,919,343 | 4,634 |
| ENST00000588802.5 | hg38 | chr19 | 44,914,325 | 44,919,346 | 5,022 |
| ENST00000588750.5 | hg38 | chr19 | 44,914,247 | 44,919,342 | 5,096 |
| ENST00000592535.6 | hg38 | chr19 | 44,914,608 | 44,919,346 | 4,739 |
| ENST00000586638.5 | hg38 | chr19 | 44,914,869 | 44,919,346 | 4,478 |
| ENST00000588750.5 | hg19 | chr19 | 45,417,504 | 45,422,599 | 5,096 |
| ENST00000588802.5 | hg19 | chr19 | 45,417,582 | 45,422,603 | 5,022 |
| ENST00000592535.6 | hg19 | chr19 | 45,417,865 | 45,422,603 | 4,739 |
| ENST00000592885.5 | hg19 | chr19 | 45,417,960 | 45,422,601 | 4,642 |
| ENST00000589781.1 | hg19 | chr19 | 45,417,967 | 45,422,600 | 4,634 |
| ENST00000586638.5 | hg19 | chr19 | 45,418,126 | 45,422,603 | 4,478 |
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