ATF5 activating transcription factor 5
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 4 |
Uncertain significance | 0 | 10 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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14 |
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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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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 | ATFX |
SYNONYM | HMFN0395 |
MIM | 606398 OMIM |
HGNC | HGNC:790 HGNC |
Ensembl | ENSG00000169136 Ensembl |
AllianceGenome | HGNC:790 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000423777.7 | hg38 | chr19 | 49,929,205 | 49,933,935 | 4,731 |
ENST00000595125.5 | hg38 | chr19 | 49,928,702 | 49,933,298 | 4,597 |
ENST00000600336.1 | hg38 | chr19 | 49,929,217 | 49,931,229 | 2,013 |
ENST00000595125.5 | hg19 | chr19 | 50,431,959 | 50,436,555 | 4,597 |
ENST00000423777.7 | hg19 | chr19 | 50,432,462 | 50,437,192 | 4,731 |
ENST00000600336.1 | hg19 | chr19 | 50,432,474 | 50,434,486 | 2,013 |
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