SYT5 synaptotagmin 5
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Uncertain significance | 0 | 36 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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36 |
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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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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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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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MIM | 600782 OMIM |
HGNC | HGNC:11513 HGNC |
Ensembl | ENSG00000129990 Ensembl |
AllianceGenome | HGNC:11513 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000354308.8 | hg38 | chr19 | 55,171,196 | 55,180,289 | 9,094 |
ENST00000590851.5 | hg38 | chr19 | 55,171,199 | 55,179,390 | 8,192 |
ENST00000537500.5 | hg38 | chr19 | 55,173,096 | 55,180,104 | 7,009 |
ENST00000354308.8 | hg19 | chr19 | 55,682,564 | 55,691,657 | 9,094 |
ENST00000590851.5 | hg19 | chr19 | 55,682,567 | 55,690,758 | 8,192 |
ENST00000537500.5 | hg19 | chr19 | 55,684,464 | 55,691,472 | 7,009 |
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