CTDSP2 CTD small phosphatase 2
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 8 |
Uncertain significance | 0 | 8 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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16 |
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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
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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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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 | OS4 |
SYNONYM | PSR2 |
SYNONYM | SCP2 |
MIM | 608711 OMIM |
HGNC | HGNC:17077 HGNC |
Ensembl | ENSG00000175215 Ensembl |
AllianceGenome | HGNC:17077 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000398073.7 | hg38 | chr12 | 57,819,927 | 57,846,729 | 26,803 |
ENST00000547701.5 | hg38 | chr12 | 57,823,461 | 57,845,534 | 22,074 |
ENST00000548823.1 | hg38 | chr12 | 57,822,800 | 57,846,704 | 23,905 |
ENST00000398073.7 | hg19 | chr12 | 58,213,710 | 58,240,512 | 26,803 |
ENST00000548823.1 | hg19 | chr12 | 58,216,583 | 58,240,487 | 23,905 |
ENST00000547701.5 | hg19 | chr12 | 58,217,244 | 58,239,317 | 22,074 |
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