NUDT7 nudix hydrolase 7
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 2 |
Likely benign | 0 | 4 |
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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38 |
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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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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 |
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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 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000563839.1 | hg38 | chr16 | 77,722,545 | 77,741,824 | 19,280 |
ENST00000437314.3 | hg38 | chr16 | 77,722,519 | 77,742,258 | 19,740 |
ENST00000568787.5 | hg38 | chr16 | 77,722,516 | 77,736,249 | 13,734 |
ENST00000268533.9 | hg38 | chr16 | 77,722,514 | 77,742,260 | 19,747 |
ENST00000564085.5 | hg38 | chr16 | 77,722,514 | 77,741,969 | 19,456 |
ENST00000613075.4 | hg38 | chr16 | 77,722,492 | 77,742,260 | 19,769 |
ENST00000613075.4 | hg19 | chr16 | 77,756,389 | 77,776,157 | 19,769 |
ENST00000564085.5 | hg19 | chr16 | 77,756,411 | 77,775,866 | 19,456 |
ENST00000268533.9 | hg19 | chr16 | 77,756,411 | 77,776,157 | 19,747 |
ENST00000568787.5 | hg19 | chr16 | 77,756,413 | 77,770,146 | 13,734 |
ENST00000437314.3 | hg19 | chr16 | 77,756,416 | 77,776,155 | 19,740 |
ENST00000563839.1 | hg19 | chr16 | 77,756,442 | 77,775,721 | 19,280 |
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