KAT7 lysine acetyltransferase 7
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 2 |
Uncertain significance | 0 | 38 |
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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2 |
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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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 |
Type | ID |
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SYNONYM | HBO1 |
SYNONYM | HBOA |
SYNONYM | MYST2 |
SYNONYM | ZC2HC7 |
MIM | 609880 OMIM |
HGNC | HGNC:17016 HGNC |
Ensembl | ENSG00000136504 Ensembl |
AllianceGenome | HGNC:17016 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000424009.6 | hg38 | chr17 | 49,788,706 | 49,829,096 | 40,391 |
ENST00000514540.6 | hg38 | chr17 | 49,815,031 | 49,827,555 | 12,525 |
ENST00000706513.1 | hg38 | chr17 | 49,788,675 | 49,829,089 | 40,415 |
ENST00000435742.2 | hg38 | chr17 | 49,789,653 | 49,829,096 | 39,444 |
ENST00000710381.1 | hg38 | chr17 | 49,788,681 | 49,835,026 | 46,346 |
ENST00000706509.1 | hg38 | chr17 | 49,788,648 | 49,829,089 | 40,442 |
ENST00000706508.1 | hg38 | chr17 | 49,788,648 | 49,829,089 | 40,442 |
ENST00000706506.1 | hg38 | chr17 | 49,788,624 | 49,832,771 | 44,148 |
ENST00000706511.1 | hg38 | chr17 | 49,788,649 | 49,829,089 | 40,441 |
ENST00000510819.5 | hg38 | chr17 | 49,788,693 | 49,827,800 | 39,108 |
ENST00000503635.2 | hg38 | chr17 | 49,788,648 | 49,827,248 | 38,601 |
ENST00000259021.9 | hg38 | chr17 | 49,788,681 | 49,835,026 | 46,346 |
ENST00000454930.6 | hg38 | chr17 | 49,788,681 | 49,827,703 | 39,023 |
ENST00000706637.1 | hg38 | chr17 | 49,788,675 | 49,829,089 | 40,415 |
ENST00000706642.1 | hg38 | chr17 | 49,820,788 | 49,829,089 | 8,302 |
ENST00000706640.1 | hg38 | chr17 | 49,788,693 | 49,829,089 | 40,397 |
ENST00000509773.5 | hg38 | chr17 | 49,788,682 | 49,827,617 | 38,936 |
ENST00000706629.1 | hg38 | chr17 | 49,788,675 | 49,829,089 | 40,415 |
ENST00000506533.6 | hg38 | chr17 | 49,789,312 | 49,829,232 | 39,921 |
ENST00000503635.2 | hg19 | chr17 | 47,866,010 | 47,904,610 | 38,601 |
ENST00000509773.5 | hg19 | chr17 | 47,866,044 | 47,904,979 | 38,936 |
ENST00000424009.6 | hg19 | chr17 | 47,866,068 | 47,906,458 | 40,391 |
ENST00000435742.2 | hg19 | chr17 | 47,867,015 | 47,906,458 | 39,444 |
ENST00000506533.6 | hg19 | chr17 | 47,866,674 | 47,906,594 | 39,921 |
ENST00000706506.1 | hg19 | chr17 | 47,865,986 | 47,910,133 | 44,148 |
ENST00000710381.1 | hg19 | chr17 | 47,866,043 | 47,912,388 | 46,346 |
ENST00000259021.9 | hg19 | chr17 | 47,866,043 | 47,912,388 | 46,346 |
ENST00000454930.6 | hg19 | chr17 | 47,866,043 | 47,905,065 | 39,023 |
ENST00000706637.1 | hg19 | chr17 | 47,866,037 | 47,906,451 | 40,415 |
ENST00000706508.1 | hg19 | chr17 | 47,866,010 | 47,906,451 | 40,442 |
ENST00000706509.1 | hg19 | chr17 | 47,866,010 | 47,906,451 | 40,442 |
ENST00000706511.1 | hg19 | chr17 | 47,866,011 | 47,906,451 | 40,441 |
ENST00000510819.5 | hg19 | chr17 | 47,866,055 | 47,905,162 | 39,108 |
ENST00000514540.6 | hg19 | chr17 | 47,892,393 | 47,904,917 | 12,525 |
ENST00000706513.1 | hg19 | chr17 | 47,866,037 | 47,906,451 | 40,415 |
ENST00000706629.1 | hg19 | chr17 | 47,866,037 | 47,906,451 | 40,415 |
ENST00000706640.1 | hg19 | chr17 | 47,866,055 | 47,906,451 | 40,397 |
ENST00000706642.1 | hg19 | chr17 | 47,898,150 | 47,906,451 | 8,302 |
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