NOX1 NADPH oxidase 1
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 6 |
Likely benign | 0 | 28 |
not provided | 6 | 0 |
Uncertain significance | 0 | 48 |
Ranking
ClinVar | |
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0 |
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0 |
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10 |
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72 |
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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
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 |
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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 |
Search Word
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 | GP91-2 |
SYNONYM | MOX1 |
SYNONYM | NOH-1 |
SYNONYM | NOH-1L |
SYNONYM | NOH1 |
MIM | 300225 OMIM |
HGNC | HGNC:7889 HGNC |
Ensembl | ENSG00000007952 Ensembl |
AllianceGenome | HGNC:7889 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000372960.8 | hg38 | chrX | 100,843,324 | 100,874,345 | 31,022 |
ENST00000372964.5 | hg38 | chrX | 100,843,333 | 100,874,209 | 30,877 |
ENST00000372966.8 | hg38 | chrX | 100,843,324 | 100,874,359 | 31,036 |
ENST00000217885.5 | hg38 | chrX | 100,843,836 | 100,874,209 | 30,374 |
ENST00000372960.8 | hg19 | chrX | 100,098,313 | 100,129,334 | 31,022 |
ENST00000372966.8 | hg19 | chrX | 100,098,313 | 100,129,348 | 31,036 |
ENST00000372964.5 | hg19 | chrX | 100,098,322 | 100,129,198 | 30,877 |
ENST00000217885.5 | hg19 | chrX | 100,098,825 | 100,129,198 | 30,374 |
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