SPTY2D1 SPT2 chromatin protein domain containing 1
Information
- Symbol
- SPTY2D1
- Type
- protein-coding
- Description
- SPT2 chromatin protein domain containing 1
- Entrez Gene ID
- 144108
- Genome
- hg19
- Position
- chr11:18,627,950-18,655,889
- Genome
- hg38
- Position
- chr11:18,606,403-18,634,342
- HGNC
- HGNC:26818 HGNC
- Ensembl
- ENSG00000179119 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 6 |
Uncertain significance | 0 | 70 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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76 |
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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
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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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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 |
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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 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000336349.6 | hg38 | chr11 | 18,606,403 | 18,634,342 | 27,940 |
ENST00000336349.6 | hg19 | chr11 | 18,627,950 | 18,655,889 | 27,940 |
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