RAD51AP1 RAD51 associated protein 1
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 10 |
Likely benign | 0 | 6 |
Uncertain significance | 0 | 34 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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50 |
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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
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 |
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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 |
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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 | PIR51 |
MIM | 603070 OMIM |
HGNC | HGNC:16956 HGNC |
Ensembl | ENSG00000111247 Ensembl |
AllianceGenome | HGNC:16956 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000352618.9 | hg38 | chr12 | 4,538,890 | 4,560,047 | 21,158 |
ENST00000228843.13 | hg38 | chr12 | 4,538,890 | 4,560,047 | 21,158 |
ENST00000544927.5 | hg38 | chr12 | 4,538,930 | 4,558,970 | 20,041 |
ENST00000228843.13 | hg19 | chr12 | 4,648,056 | 4,669,213 | 21,158 |
ENST00000352618.9 | hg19 | chr12 | 4,648,056 | 4,669,213 | 21,158 |
ENST00000544927.5 | hg19 | chr12 | 4,648,096 | 4,668,136 | 20,041 |
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