VAT1 vesicle amine transport 1
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 2 |
Likely benign | 0 | 2 |
Uncertain significance | 0 | 32 |
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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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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SYNONYM | VATI |
MIM | 604631 OMIM |
HGNC | HGNC:16919 HGNC |
Ensembl | ENSG00000108828 Ensembl |
AllianceGenome | HGNC:16919 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000355653.8 | hg38 | chr17 | 43,014,607 | 43,022,385 | 7,779 |
ENST00000420567.7 | hg38 | chr17 | 43,015,918 | 43,020,273 | 4,356 |
ENST00000587173.5 | hg38 | chr17 | 43,015,899 | 43,022,356 | 6,458 |
ENST00000355653.8 | hg19 | chr17 | 41,166,624 | 41,174,402 | 7,779 |
ENST00000587173.5 | hg19 | chr17 | 41,167,916 | 41,174,373 | 6,458 |
ENST00000420567.7 | hg19 | chr17 | 41,167,935 | 41,172,290 | 4,356 |
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