ATG9B autophagy related 9B
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely pathogenic | 0 | 2 |
Likely benign | 0 | 10 |
Uncertain significance | 0 | 104 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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116 |
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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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SYNONYM | APG9L2 |
SYNONYM | NOS3AS |
SYNONYM | SONE |
MIM | 612205 OMIM |
HGNC | HGNC:21899 HGNC |
Ensembl | ENSG00000181652 Ensembl |
AllianceGenome | HGNC:21899 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000469530.4 | hg38 | chr7 | 151,015,182 | 151,024,423 | 9,242 |
ENST00000639579.2 | hg38 | chr7 | 151,015,151 | 151,024,494 | 9,344 |
ENST00000639579.2 | hg19 | chr7 | 150,712,239 | 150,721,581 | 9,343 |
ENST00000469530.4 | hg19 | chr7 | 150,712,270 | 150,721,510 | 9,241 |
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