ANAPC7 anaphase promoting complex subunit 7
Information
- Symbol
- ANAPC7
- Type
- protein-coding
- Description
- anaphase promoting complex subunit 7
- Entrez Gene ID
- 51434
- Genome
- hg19
- Position
- chr12:110,810,705-110,841,513
- Genome
- hg38
- Position
- chr12:110,372,900-110,403,708
- MIM
- 606949 OMIM
- HGNC
- HGNC:17380 HGNC
- Ensembl
- ENSG00000196510 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Uncertain significance | 0 | 24 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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24 |
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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 |
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Entry | Origin | Type | Annotation | Entry | Origin | Annotation |
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Target data | : |
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 |
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 | |||
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Entry | Origin | Type | Annotation |
Type | ID |
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SYNONYM | APC7 |
SYNONYM | FERBON |
MIM | 606949 OMIM |
HGNC | HGNC:17380 HGNC |
Ensembl | ENSG00000196510 Ensembl |
AllianceGenome | HGNC:17380 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000450008.3 | hg38 | chr12 | 110,375,477 | 110,403,730 | 28,254 |
ENST00000455511.9 | hg38 | chr12 | 110,372,900 | 110,403,708 | 30,809 |
ENST00000455511.9 | hg19 | chr12 | 110,810,705 | 110,841,513 | 30,809 |
ENST00000450008.3 | hg19 | chr12 | 110,813,282 | 110,841,535 | 28,254 |
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