CSAG1 chondrosarcoma associated gene 1
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 1 |
Likely benign | 0 | 2 |
not provided | 6 | 0 |
Uncertain significance | 0 | 12 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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15 |
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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
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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 |
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 | CSAGE |
SYNONYM | CT24.1 |
MIM | 300944 OMIM |
HGNC | HGNC:24294 HGNC |
Ensembl | ENSG00000198930 Ensembl |
AllianceGenome | HGNC:24294 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000370291.6 | hg38 | chrX | 152,727,484 | 152,733,691 | 6,208 |
ENST00000452779.3 | hg38 | chrX | 152,727,484 | 152,733,721 | 6,238 |
ENST00000370287.7 | hg38 | chrX | 152,727,484 | 152,733,735 | 6,252 |
ENST00000370287.7 | hg19 | chrX | 151,903,228 | 151,909,518 | 6,291 |
ENST00000370291.6 | hg19 | chrX | 151,903,272 | 151,909,518 | 6,247 |
ENST00000452779.3 | hg19 | chrX | 151,903,242 | 151,909,518 | 6,277 |
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