ASB16 ankyrin repeat and SOCS box containing 16
Information
- Symbol
- ASB16
- Type
- protein-coding
- Description
- ankyrin repeat and SOCS box containing 16
- Entrez Gene ID
- 92591
- Genome
- hg19
- Position
- chr17:42,248,072-42,256,452
- Genome
- hg38
- Position
- chr17:44,170,704-44,179,084
- MIM
- 615056 OMIM
- HGNC
- HGNC:19768 HGNC
- Ensembl
- ENSG00000161664 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 12 |
Conflicting classifications of pathogenicity | 0 | 2 |
Uncertain significance | 0 | 66 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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78 |
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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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Search word | : | |
Filtering | : |
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 |
---|---|
MIM | 615056 OMIM |
HGNC | HGNC:19768 HGNC |
Ensembl | ENSG00000161664 Ensembl |
AllianceGenome | HGNC:19768 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000293414.6 | hg38 | chr17 | 44,170,704 | 44,179,084 | 8,381 |
ENST00000293414.6 | hg19 | chr17 | 42,248,072 | 42,256,452 | 8,381 |
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