TADA3 transcriptional adaptor 3
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 4 |
Uncertain significance | 0 | 30 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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34 |
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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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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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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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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 | ADA3 |
SYNONYM | NGG1 |
SYNONYM | STAF54 |
SYNONYM | TADA3L |
SYNONYM | hADA3 |
MIM | 602945 OMIM |
HGNC | HGNC:19422 HGNC |
Ensembl | ENSG00000171148 Ensembl |
AllianceGenome | HGNC:19422 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000343450.2 | hg38 | chr3 | 9,783,128 | 9,792,736 | 9,609 |
ENST00000301964.7 | hg38 | chr3 | 9,779,967 | 9,792,473 | 12,507 |
ENST00000440161.5 | hg38 | chr3 | 9,780,256 | 9,793,011 | 12,756 |
ENST00000301964.7 | hg19 | chr3 | 9,821,651 | 9,834,157 | 12,507 |
ENST00000440161.5 | hg19 | chr3 | 9,821,940 | 9,834,695 | 12,756 |
ENST00000343450.2 | hg19 | chr3 | 9,824,812 | 9,834,420 | 9,609 |
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