SPRY2 sprouty RTK signaling antagonist 2
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 4 |
Likely benign | 0 | 2 |
risk factor | 0 | 2 |
Uncertain significance | 0 | 30 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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36 |
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2 |
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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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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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 | IGAN3 |
SYNONYM | hSPRY2 |
MIM | 602466 OMIM |
HGNC | HGNC:11270 HGNC |
Ensembl | ENSG00000136158 Ensembl |
AllianceGenome | HGNC:11270 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000377102.5 | hg38 | chr13 | 80,335,976 | 80,339,659 | 3,684 |
ENST00000377104.4 | hg38 | chr13 | 80,335,976 | 80,341,126 | 5,151 |
ENST00000377102.5 | hg19 | chr13 | 80,910,111 | 80,913,794 | 3,684 |
ENST00000377104.4 | hg19 | chr13 | 80,910,111 | 80,915,261 | 5,151 |
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