SIRT2 sirtuin 2
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 12 |
Likely benign | 0 | 2 |
Uncertain significance | 0 | 60 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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74 |
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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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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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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 |
Type | ID |
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SYNONYM | SIR2 |
SYNONYM | SIR2L |
SYNONYM | SIR2L2 |
MIM | 604480 OMIM |
HGNC | HGNC:10886 HGNC |
Ensembl | ENSG00000068903 Ensembl |
AllianceGenome | HGNC:10886 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000249396.12 | hg38 | chr19 | 38,878,560 | 38,899,618 | 21,059 |
ENST00000358931.9 | hg38 | chr19 | 38,878,555 | 38,899,862 | 21,308 |
ENST00000392081.6 | hg38 | chr19 | 38,878,557 | 38,899,862 | 21,306 |
ENST00000358931.9 | hg19 | chr19 | 39,369,195 | 39,390,502 | 21,308 |
ENST00000249396.12 | hg19 | chr19 | 39,369,200 | 39,390,258 | 21,059 |
ENST00000392081.6 | hg19 | chr19 | 39,369,197 | 39,390,502 | 21,306 |
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