DPYSL5 dihydropyrimidinase like 5
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 6 |
Likely benign | 0 | 22 |
Conflicting classifications of pathogenicity | 0 | 4 |
Uncertain significance | 0 | 60 |
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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4 |
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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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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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 | CRAM |
SYNONYM | CRMP-5 |
SYNONYM | CRMP5 |
SYNONYM | CV2 |
SYNONYM | RTSC4 |
SYNONYM | Ulip6 |
MIM | 608383 OMIM |
HGNC | HGNC:20637 HGNC |
Ensembl | ENSG00000157851 Ensembl |
AllianceGenome | HGNC:20637 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000614712.4 | hg38 | chr2 | 26,848,424 | 26,950,350 | 101,927 |
ENST00000401478.5 | hg38 | chr2 | 26,848,289 | 26,947,197 | 98,909 |
ENST00000288699.11 | hg38 | chr2 | 26,848,132 | 26,950,351 | 102,220 |
ENST00000288699.11 | hg19 | chr2 | 27,071,000 | 27,173,219 | 102,220 |
ENST00000401478.5 | hg19 | chr2 | 27,071,157 | 27,170,065 | 98,909 |
ENST00000614712.4 | hg19 | chr2 | 27,071,292 | 27,173,218 | 101,927 |
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