ANKRD33 ankyrin repeat domain 33
Information
- Symbol
- ANKRD33
- Type
- protein-coding
- Description
- ankyrin repeat domain 33
- Entrez Gene ID
- 341405
- Genome
- hg19
- Position
- chr12:52,281,887-52,285,511
- Genome
- hg38
- Position
- chr12:51,888,103-51,891,727
- HGNC
- HGNC:13788 HGNC
- Ensembl
- ENSG00000167612 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 2 |
Uncertain significance | 0 | 56 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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58 |
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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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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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Category | : |
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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 | C12orf7 |
SYNONYM | PANKY |
HGNC | HGNC:13788 HGNC |
Ensembl | ENSG00000167612 Ensembl |
AllianceGenome | HGNC:13788 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000340970.8 | hg38 | chr12 | 51,888,217 | 51,891,657 | 3,441 |
ENST00000301190.11 | hg38 | chr12 | 51,888,103 | 51,891,727 | 3,625 |
ENST00000301190.11 | hg19 | chr12 | 52,281,887 | 52,285,511 | 3,625 |
ENST00000340970.8 | hg19 | chr12 | 52,282,001 | 52,285,441 | 3,441 |
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