NAT9 N-acetyltransferase 9 (putative)
Information
- Symbol
- NAT9
- Type
- protein-coding
- Description
- N-acetyltransferase 9 (putative)
- Entrez Gene ID
- 26151
- Genome
- hg19
- Position
- chr17:72,767,834-72,772,437
- Genome
- hg38
- Position
- chr17:74,771,695-74,776,298
- HGNC
- HGNC:23133 HGNC
- Ensembl
- ENSG00000109065 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Uncertain significance | 0 | 16 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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16 |
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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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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 | EBSP, hNATL |
HGNC | HGNC:23133 HGNC |
Ensembl | ENSG00000109065 Ensembl |
AllianceGenome | HGNC:23133 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000581136.5 | hg38 | chr17 | 74,771,389 | 74,776,324 | 4,936 |
ENST00000582870.5 | hg38 | chr17 | 74,771,660 | 74,776,323 | 4,664 |
ENST00000580632.5 | hg38 | chr17 | 74,771,558 | 74,775,707 | 4,150 |
ENST00000582524.5 | hg38 | chr17 | 74,771,764 | 74,776,365 | 4,602 |
ENST00000357814.8 | hg38 | chr17 | 74,770,529 | 74,776,345 | 5,817 |
ENST00000578822.5 | hg38 | chr17 | 74,771,695 | 74,776,298 | 4,604 |
ENST00000583476.5 | hg38 | chr17 | 74,771,768 | 74,776,337 | 4,570 |
ENST00000580301.5 | hg38 | chr17 | 74,770,567 | 74,776,339 | 5,773 |
ENST00000583757.5 | hg38 | chr17 | 74,771,728 | 74,776,342 | 4,615 |
ENST00000357814.8 | hg19 | chr17 | 72,766,668 | 72,772,484 | 5,817 |
ENST00000578822.5 | hg19 | chr17 | 72,767,834 | 72,772,437 | 4,604 |
ENST00000580301.5 | hg19 | chr17 | 72,766,706 | 72,772,478 | 5,773 |
ENST00000580632.5 | hg19 | chr17 | 72,767,697 | 72,771,846 | 4,150 |
ENST00000581136.5 | hg19 | chr17 | 72,767,528 | 72,772,463 | 4,936 |
ENST00000582524.5 | hg19 | chr17 | 72,767,903 | 72,772,504 | 4,602 |
ENST00000582870.5 | hg19 | chr17 | 72,767,799 | 72,772,462 | 4,664 |
ENST00000583476.5 | hg19 | chr17 | 72,767,907 | 72,772,476 | 4,570 |
ENST00000583757.5 | hg19 | chr17 | 72,767,867 | 72,772,481 | 4,615 |
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