QPRT quinolinate phosphoribosyltransferase
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 14 |
Likely benign | 0 | 18 |
not provided | 9 | 0 |
Uncertain significance | 0 | 74 |
Ranking
ClinVar | |
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0 |
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0 |
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6 |
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100 |
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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 | HEL-S-90n |
SYNONYM | QPRTase |
MIM | 606248 OMIM |
HGNC | HGNC:9755 HGNC |
Ensembl | ENSG00000103485 Ensembl |
AllianceGenome | HGNC:9755 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000562473.1 | hg38 | chr16 | 29,679,182 | 29,697,524 | 18,343 |
ENST00000449759.2 | hg38 | chr16 | 29,663,279 | 29,697,638 | 34,360 |
ENST00000395384.9 | hg38 | chr16 | 29,679,180 | 29,698,699 | 19,520 |
ENST00000449759.2 | hg19 | chr16 | 29,674,600 | 29,708,959 | 34,360 |
ENST00000395384.9 | hg19 | chr16 | 29,690,501 | 29,710,020 | 19,520 |
ENST00000562473.1 | hg19 | chr16 | 29,690,503 | 29,708,845 | 18,343 |
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