ARID3B AT-rich interaction domain 3B
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 6 |
Likely benign | 0 | 2 |
not provided | 2 | 0 |
Uncertain significance | 0 | 40 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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48 |
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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
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 |
Search Word
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 | BDP |
SYNONYM | DRIL2 |
MIM | 612457 OMIM |
HGNC | HGNC:14350 HGNC |
Ensembl | ENSG00000179361 Ensembl |
AllianceGenome | HGNC:14350 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000622429.1 | hg38 | chr15 | 74,541,206 | 74,598,129 | 56,924 |
ENST00000346246.10 | hg38 | chr15 | 74,541,220 | 74,598,131 | 56,912 |
ENST00000622429.1 | hg19 | chr15 | 74,833,547 | 74,890,470 | 56,924 |
ENST00000346246.10 | hg19 | chr15 | 74,833,561 | 74,890,472 | 56,912 |
Key | Value |
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strand | + |
UniProt | TSG |
start | 74,833,517 |
Gene Symbol | ARID3B |
Entrez GeneId | 10,620 |
Chr Band | 15q24 |
end | 74,890,471 |
chr | chr15 |
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