NQO1 NAD(P)H quinone dehydrogenase 1
Information
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Likely pathogenic | 0 | 4 |
| Benign | 0 | 6 |
| Likely benign | 0 | 234 |
| Uncertain significance | 0 | 220 |
Ranking
| ClinVar | |
|---|---|
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0 |
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0 |
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6 |
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456 |
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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 | |||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | |||||||||||||||
| Type | ID |
|---|---|
| SYNONYM | DHQU |
| SYNONYM | DIA4 |
| SYNONYM | DTD |
| SYNONYM | NMOR1 |
| SYNONYM | NMORI |
| SYNONYM | QR1 |
| MIM | 125860 OMIM |
| HGNC | HGNC:2874 HGNC |
| Ensembl | ENSG00000181019 Ensembl |
| AllianceGenome | HGNC:2874 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000379046.6 | hg38 | chr16 | 69,710,727 | 69,726,584 | 15,858 |
| ENST00000379047.7 | hg38 | chr16 | 69,709,401 | 69,726,668 | 17,268 |
| ENST00000564043.1 | hg38 | chr16 | 69,710,962 | 69,726,560 | 15,599 |
| ENST00000320623.10 | hg38 | chr16 | 69,709,401 | 69,726,560 | 17,160 |
| ENST00000439109.6 | hg38 | chr16 | 69,710,782 | 69,726,560 | 15,779 |
| ENST00000561500.5 | hg38 | chr16 | 69,706,996 | 69,726,506 | 19,511 |
| ENST00000561500.5 | hg19 | chr16 | 69,740,899 | 69,760,409 | 19,511 |
| ENST00000320623.10 | hg19 | chr16 | 69,743,304 | 69,760,463 | 17,160 |
| ENST00000379047.7 | hg19 | chr16 | 69,743,304 | 69,760,571 | 17,268 |
| ENST00000379046.6 | hg19 | chr16 | 69,744,630 | 69,760,487 | 15,858 |
| ENST00000439109.6 | hg19 | chr16 | 69,744,685 | 69,760,463 | 15,779 |
| ENST00000564043.1 | hg19 | chr16 | 69,744,865 | 69,760,463 | 15,599 |
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