ARID5A AT-rich interaction domain 5A
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 10 |
not provided | 2 | 0 |
Uncertain significance | 0 | 78 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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88 |
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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 | MRF-1 |
SYNONYM | MRF1 |
SYNONYM | RP11-363D14 |
MIM | 611583 OMIM |
HGNC | HGNC:17361 HGNC |
Ensembl | ENSG00000196843 Ensembl |
AllianceGenome | HGNC:17361 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000673792.1 | hg38 | chr2 | 96,536,752 | 96,552,396 | 15,645 |
ENST00000357485.8 | hg38 | chr2 | 96,536,752 | 96,552,634 | 15,883 |
ENST00000454558.2 | hg38 | chr2 | 96,537,345 | 96,552,634 | 15,290 |
ENST00000673792.1 | hg19 | chr2 | 97,202,489 | 97,218,133 | 15,645 |
ENST00000357485.8 | hg19 | chr2 | 97,202,489 | 97,218,371 | 15,883 |
ENST00000454558.2 | hg19 | chr2 | 97,203,082 | 97,218,371 | 15,290 |
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