STX6 syntaxin 6
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 2 |
Uncertain significance | 0 | 28 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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30 |
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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 |
Search Word
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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MIM | 603944 OMIM |
HGNC | HGNC:11441 HGNC |
Ensembl | ENSG00000135823 Ensembl |
AllianceGenome | HGNC:11441 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000258301.6 | hg38 | chr1 | 180,972,725 | 181,022,870 | 50,146 |
ENST00000542060.5 | hg38 | chr1 | 180,972,712 | 181,023,121 | 50,410 |
ENST00000542060.5 | hg19 | chr1 | 180,941,848 | 180,992,257 | 50,410 |
ENST00000258301.6 | hg19 | chr1 | 180,941,861 | 180,992,006 | 50,146 |
Genome browser