NKAPD1 NKAP domain containing 1
Information
- Symbol
- NKAPD1
- Type
- protein-coding
- Description
- NKAP domain containing 1
- Entrez Gene ID
- 55216
- Genome
- hg19
- Position
- chr11:111,945,023-111,955,874
- Genome
- hg38
- Position
- chr11:112,074,299-112,085,150
- HGNC
- HGNC:25569 HGNC
- Ensembl
- ENSG00000150776 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Uncertain significance | 0 | 4 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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4 |
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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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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 | C11orf57 |
HGNC | HGNC:25569 HGNC |
Ensembl | ENSG00000150776 Ensembl |
AllianceGenome | HGNC:25569 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000393047.8 | hg38 | chr11 | 112,074,299 | 112,085,150 | 10,852 |
ENST00000420986.6 | hg38 | chr11 | 112,074,086 | 112,084,134 | 10,049 |
ENST00000532163.5 | hg38 | chr11 | 112,074,287 | 112,085,150 | 10,864 |
ENST00000280352.13 | hg38 | chr11 | 112,074,289 | 112,085,150 | 10,862 |
ENST00000420986.6 | hg19 | chr11 | 111,944,810 | 111,954,858 | 10,049 |
ENST00000532163.5 | hg19 | chr11 | 111,945,011 | 111,955,874 | 10,864 |
ENST00000280352.13 | hg19 | chr11 | 111,945,013 | 111,955,874 | 10,862 |
ENST00000393047.8 | hg19 | chr11 | 111,945,023 | 111,955,874 | 10,852 |
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