NAP1L4 nucleosome assembly protein 1 like 4
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 2 |
Likely benign | 0 | 4 |
Uncertain significance | 0 | 44 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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50 |
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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 | |||||
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Entry | Origin | Type | Annotation | Entry | Origin | Annotation |
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Target data | : |
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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Category | : |
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Search word | : | |
Filtering | : |
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 |
---|---|
SYNONYM | NAP1L4b |
SYNONYM | NAP2 |
SYNONYM | NAP2L |
SYNONYM | hNAP2 |
MIM | 601651 OMIM |
HGNC | HGNC:7640 HGNC |
Ensembl | ENSG00000205531 Ensembl |
AllianceGenome | HGNC:7640 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000380542.9 | hg38 | chr11 | 2,944,437 | 2,992,329 | 47,893 |
ENST00000703798.1 | hg38 | chr11 | 2,944,437 | 2,992,292 | 47,856 |
ENST00000526115.5 | hg38 | chr11 | 2,945,112 | 2,992,377 | 47,266 |
ENST00000448187.6 | hg38 | chr11 | 2,944,444 | 2,992,300 | 47,857 |
ENST00000620138.4 | hg38 | chr11 | 2,944,431 | 2,992,377 | 47,947 |
ENST00000380542.9 | hg19 | chr11 | 2,965,667 | 3,013,559 | 47,893 |
ENST00000448187.6 | hg19 | chr11 | 2,965,674 | 3,013,530 | 47,857 |
ENST00000526115.5 | hg19 | chr11 | 2,966,342 | 3,013,607 | 47,266 |
ENST00000620138.4 | hg19 | chr11 | 2,965,661 | 3,013,607 | 47,947 |
ENST00000703798.1 | hg19 | chr11 | 2,965,667 | 3,013,522 | 47,856 |
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